22nd Annual Clinical Trial Supply East Coast 2024

Covering all things CTS from reducing timelines and streamlining processes to handling clinical supplies in a decentralized trial world.

5 - 6

November

2024
  • Sheraton Valley Forge, King of Prussia, PA, USA
  • Free
  • Why attend?
  • Agenda
  • Advisory Board
  • Speakers
  • Plan Your Visit
  • Event Gallery
  • Sponsors
  • Media Centre
  • Why partner?
  • Contact Us
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2023 Sponsors Include:

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Company Information

Clinical Services International (CSI) is a global leader of sourcing and management of commercially available medicines (comparators, concomitant medication) for clinical trials.
Headquartered in London and with operations in UK, Germany, Denmark, Japan and USA, we provide efficient solutions and serve worldwide trials. Our longstanding experience and relationships with manufacturers, enables us to provide custom made solutions to address the most complex requirements.
We accelerate drug development and reduce timelines by providing a fully integrated service.
Address Regulatory, Quality, Operational, Clinical requirements
Manage the entire supply chain and offer tailor-made solutions
Comprehensive expertise in Oncology and Biosimilar products.
Advanced Technology and Innovative approach
Trusted partner of leading Biopharmaceuticals, CROs and CMOs.
www.csint.com

Company Website

To learn more, please visit our website - www.csint.com

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Company Information

Abacus Medicine Clinical Trial Services is part of The Abacus Medicine Group. Abacus Medicine was founded in 2004 by CEO Flemming Wagner to improve access to original prescription medicines throughout Europe.  Over the past five years, to expand its geographic footprint to the USA and APAC regions, the company has developed a range of Clinical Trial Services including tailored comparator sourcing and clinical packaging & labelling.

Company Website

To learn more, please visit our website - https://www.abacusmedicine-cts.com/

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Company Information

Acnos Pharma is privately-owned, specialized pharmaceutical company operating globally in the clinical trial supply landscape. The headquarter is in Germany, Aachen. We offer flexible, cost efficient and quality sensitive customized solutions for individual trial requirements. We offer a broad range of clinical trial services supply chain management, clinical trial procurement and logistics.

Th combination of passion and expertise leverages our global reach and maximizes customer satisfaction.

Company Website

To learn more, please visit our website - http://acnospharma.de/

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Company Information

Simply sourcing comparators – we offer a unique blend of small company flexibility and speed, backed with the large-scale buying power of the Orifarm Group, which is one of the largest pharmaceutical suppliers in Europe. With over €1.4B products sold in 2021 and more than 4,000 unique product lines sourced on a monthly basis, we have unparalleled access to “out of market” and manufacturer direct buying capability, both in the US and Europe.

Company website: www.Orifarm-CTS.com

Company Website

To learn more, please visit our website - www.Orifarm-CTS.com

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Company Information

Sharp is a global leader in clinical supply trial services and pharmaceutical packaging. For 70 years, we’ve provided solutions to pharma and biotech clients from phase I trials through to commercial launch and lifecycle management.

Company Website

To learn more, please visit our website - http://www.sharpservices.com/

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Company Information

NULL

Company Website

To learn more, please visit our website - http://www.innovativesupplysolutions.com/

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Company Information

Veeva is a leader in cloud-based software for the global life sciences industry. Committed to innovation, product excellence and customer success, Veeva has over 150 customers, ranging from the world’s largest pharmaceutical companies to emerging biotechs.

Company Website

To learn more, please visit our website - www.veeva.com

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Company Information

BMclinical, your global clinical trial supply partner. We offer worldwide commercial medicine supply, from analytical samples to bulk comparators, through to the supply of co-meds and pre-meds.  We can pack and label your IMP/commercial medicines from our GMP facility, where we also offer storage and distribution services. BMclinical is uniquely positioned to offer solutions for overage and unused clinical trial stock.

Company Website

To learn more, please visit our website - https://www.bmclinical.com

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Company Information

Myonex provides tailored services and solutions to advance medicine through clinical to commercial stages with tailored drug sourcing and ancillary supply, to packaging, labeling, and distribution. With ten global locations, we offer flexible, efficient, and cost-effective support for clients across the pharmaceutical and biotech sectors.

 

Company Website

To learn more, please visit our website - www.myonex.com

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Company Information

Euromed Pharma deliver strategic services tailored to support companies in their quest to better healthcare. We support each industry player from drug development through the post-marketing phases. We offer solutions in CTS services, Clinical GMP Packaging, Labeling and Distribution, IMP management, Early Access and Named Patient Programs, Pharma Order to cash solutions, and Supply Chain & Logistics. We are present around the world with offices in Italy, Spain, Ireland, Germany, Singapore and the USA. Being one of the Petrone Group companies, Euromed Pharma is positioned at the forefront of innovation in pharmaceutical distribution.

Company Website

To learn more, please visit our website - www.euromed-pharma.com

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Company Website

To learn more, please visit our website - http://www.bappharma.com/

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Company Information

Bionical Emas is a global Contract Research Organization (CRO) combining Clinical Development, Clinical Trial Supply (CTS) and Early Access Programs (EAP) bringing life-changing medicines to patients around the world. Our Clinical Trial Supply Division has a global vendor network of manufacturers, wholesaler distributors and optimized sourcing strategies to support your study. Whether you require products locally sourced in emerging markets and distributed directly to trial sites, global sourcing of high-value commercial drug products, or a demand-driven sourcing approach, we have the right solution for you.

Company Website

To learn more, please visit our website - http://www.bionicalemas.com

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Company Information

Bay Area Research Logistics (BARL) is known for its superior management of clinical trial services – from drug procurement to blinding, packaging, labeling, storing and distribution. We provide seamless coordination for all sizes of trials – from large, global phase IV trials to small-scale INDs, across many therapeutic classifications ranging from Phase I to Phase IV studies.”

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Company Information

Alcami is a world-class end-to-end CDMO headquartered in North Carolina. Alcami connects its global clients with customizable and innovative solutions for API development and manufacturing, solid state chemistry, formulation development, analytical development and testing services, clinical and commercial finished dosage form manufacturing (oral solid and parenteral), packaging, and stability services.

Company Website

To learn more, please visit our website - www.alcaminow.com

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Company Information

Advarra is number one in trusted research review services, number one in innovative site and sponsor technology, and the pioneer in clinical research experience software. Our depth of technology and people expertise combine to deliver solutions that enable the collaboration, transparency, and speed required to optimize trial operations and ensure patient safety.

Company Website

To learn more, please visit our website - www.advarra.com

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    Why attend?

    We are excited to be hosting the next edition of Clinical Trial Supply East Coast to Sheraton King of Prussia.

    The conference covers all things CTS from reducing timelines and streamlining processes to handling clinical supplies in a decentralized trial world. Our expert panel will deliver case studies, thought leadership pieces, interactive panels and roundtable discussions.

    Clinical Trial Supply East Coast offers opportunities for both learning and networking with peers from across the CTS sphere, via informal networking breaks and lunches, as well as a relaxed drinks reception at the end of Day 1.

    We have the best delivery for clinical trials East Coast 2023 for which we have been chosen by online casino players among other deliveries. Also at the conferences, everything related to CTS is covered, we also talk about bills vs patriots dfs picks. Speakers from Pfizer, Merck, Janssen, online casinos and others perform on our first day.

    Our day one includes speakers from Takeda, Merck, Janssen and many more who will be covering the latest innovations in the clinical supply industry. The day will be split into two different streams, with a clinical supply operations category as well as a stream highlighting great innovation and technological updates.

    Our conference continues into day two with a stream dedicated to temperature controlled logistics as well as regulatory updates from US Customs and Border Control.

    Don’t miss out, join us in King of Prussia on the 5th and 6th of November 2024.

     

    BRINGING TOGETHER PHARMA AND BIOTECH EXPERTS TO DISCUSS NEW TRENDS AND OPPORTUNITIES

    The Clinical Trial Supply East Coast is the meeting place for the pharmaceutical and biotechnology community to discover how to excel in clinical supply strategy as well as form key connections for long-term success. It’s time to build relationships and take away valuable lessons to for clinical trial success moving forward so we look forward to seeing you there!

    300+

    Attendees

    		35+

    Exhibitors

    		20+

    Speakers
    300+

    Attendees

    		35+

    Exhibitors
    20+

    Speakers

    Testimonials

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    Agenda

    • 5 Nov 2024
    • 6 Nov 2024
    Expand All

    Streams

    Stream one

    Clinical Supply Logistics and Operations

    Stream two

    Clinical Supply Technology and Innovation

    11 AM

    PANEL: Incorporating artificial intelligence and machine learning into clinical supply chains

    • Opportunities created by AI and ML that can help optimize clinical supply chains
    • How AI and ML can help reduce costs and transit times while maintaining product integrity
    • Navigating regulatory factors linked to using AI and ML in clinical trials in the US
    • Utilizing AI to improve processes
    • Where to implement and integrate AI into supply chain processes in order to improve efficiency

    Speakers

    Maxime Derep
    Director of Solutions Engineering, N-SIDE
    Paul Hingst
    Supply Chain Consultant, Crinetics Pharmaceuticals
    Luiz Alberto Barberini
    Head of External Manufacturing, Latin America, Bayer
    Haneen Mazahreh-Boivert
    Senior Director Global Clinical Supply, Boston Pharmaceuticals

    11:30 AM

    Implementing sustainable sourcing practices for commercial medicines in your clinical trials

    • Understanding the commercial medicine supply chain inside out
    • Predicting the future: data, analytics, AI and market intelligence
    • Review regularly
    • Back-up and risk mitigation
    • Learn from experiences: case studies

    Speakers

    Ian Hoban
    Business Development Director, Abacus Medicine

    12 PM

    CASE STUDY: The e-reader for clinical trial medication: a Digital Display Labeling (DDL) system to replace traditional paper labels and booklets in clinical trials

    • Clinical supply chain evolution: using new technology to adapt
    • Understanding Digital Display Label technology and integrating it into the clinical supply chain
    • Opportunities to benefit from the flexibility the Digital Display Label system can provide
    • Transformative vision for the pharmaceutical industry

    Speakers

    Jennifer Wittman
    Associate Director, Global Clinical Supplies Project Manager, Merck

    12:30 PM

    Optimizing clinical trial supply chain efficiency through CTPAT/Trade Compliance

    • Ensuring compliance with Customs and Border Protection (CBP) regulations: a discussion of Pharmaceuticals, Health and Chemicals Center of Excellence and Expertise (PHC-CEE), the benefits of joining the CTPAT Trade Compliance (TC) program and how to become eligible
    • Strengthening supply chain security and reducing the risk of delays at the border: understanding the CBP's expectations of importers and how the CTPAT TC program can assist in meeting these requirements
    • Enhancing the efficiency of clinical trial supply management: how participation in the CTPAT TC program can streamline the import process and lead to more timely and cost-effective delivery of materials

    Speakers

    Mary Zhang
    National Account Manager, US Customs and Border Protection

    1 PM

    Lunch and networking

    2:15 PM

    How to recruit, train, and retain talent for Supply Chain 4.0

    • Addressing scarcity of supply chain talent in the market
    • Recruiting strategies: looking internally first, external hires to challenge thinking, recruiting from internal supply chain for customer-facing roles, and leveraging university co-op programs
    • Training and development should focus on comprehensive development plans, cross-functional exposure, leveraging tech eg AI/automation, encouraging risk-taking, and implementing mentorship programs
    • Diversity and inclusion: going beyond ethnicity to diversity of thought/experience, using employee resource groups, and fostering a sense of belonging
    • Building an agile team: storytelling/influencing skills, understanding the bigger picture impact, and challenging the status quo

    Speakers

    Nirav Shah
    Director, Clinical Drug Supply & Logistics

    2:45 PM

    CASE STUDY: Development and training initiatives: considerations for supply chain teams

    • An overview of Takeda’s initiatives around staff development: what worked and what didn’t?
    • Effectiveness of different recruitment, training and long term development initiatives: how did this impact sourcing and retaining talent?
    • Looking forward: evolving current training initiatives to set up for future success

    Speakers

    Paul Larochelle
    Director, Global Clinical Supply Chain, Takeda
    Sydney Reynolds
    Postdoctoral Fellow - Global Clinical Supply Chain, Takeda

    3:15 PM

    Afternoon refreshments and networking

    3:50 PM

    EXHIBITION APPLE PRIZE DRAW

    Visit our exhibitors’ booths throughout the day and collect stamps in order to enter our Prize Draw and be in for a chance of winning Apple devices or Amazon vouchers. The Prize Draw will take place in the Exhibition Hall. Make sure you don’t miss out!

    7:30 AM

    Registration and refreshments

    8:55 AM

    Chairperson’s opening remarks

    Speakers

    Amanda Murphy
    Senior Director, Data Intelligence & Solutions, GlobalData

    9 AM

    The current landscape for clinical supply chains in the US and globally

    Speakers

    Amanda Murphy
    Senior Director, Data Intelligence & Solutions, GlobalData
    Francesco Santo
    Associate Director Global Clinical Supply Chain, HUYABIO
    Chris Campbell
    Associate Director, Clinical Drug Supply and Logistics, REGENERON
    Laurie Taraborrelli
    Clinical Programs and Compliance Specialist, Fujirebio Diagnostics
    Luiz Alberto Barberini
    Head of External Manufacturing, Latin America, Bayer

    9:30 AM

    Aligning clinical supply strategies with sustainability goals

    Increasingly pharmaceutical companies are committing to reduce their carbon footprints in the execution of clinical trials. This session will cover how implementing innovative clinical trial supply technologies and sustainable processes can:

    • result in a more efficient use of human resources
    • reduce the number of logistical resources required
    • reduce waste
    • save money
    • lower the carbon footprint impact

    Speakers

    Robbie Hill
    Director, Business Development, Mercalis

    10 AM

    CASE STUDY: A journey to achieving end-to-end clinical supply chain optimization

    • What is end-to-end optimization and why does it matter?
    • Insights from a real-world case study demonstrating significant cost & efficiency gains: Sanofi’s Demand and Supply Integration Ecosystem (DASIE) project
    • Journey encompassing all supply chain actors, key benefits, impact, and integration in the overall IT landscape
    • How you can enhance your clinical supply chain performance

    Speakers

    Isaac Greenslade
    Director, Head of Demand and Supply Innovation and Transformation, Sanofi
    Pauline Deplasse
    Head of Marketing and Strategy, N-SIDE

    10:30 AM

    Morning refreshments and networking

    11 AM

    Optimizing comparator sourcing processes for your clinical trial

    • Designing your comparator sourcing strategy: key factors to consider for your clinical trial
    • Exploring strategies for reliable and cost-effective sourcing: what solutions are available?
    • Addressing regulatory considerations and compliance challenges for comparator sourcing both in the US and from overseas
    • Leveraging technology and data analytics to streamline comparator sourcing processes

    Speakers

    Francesco Santo
    Associate Director Global Clinical Supply Chain, HUYABIO

    11:30 AM

    Adapting to change: global trends, insights, and vendor relationships in modern clinical trials

    In recent years, the clinical trial landscape has undergone significant transformations driven by global events, evolving trial designs, intricate supply chains, innovative dosing schemes, and a heightened focus on patient-centric approaches. Topics discussed will explore the most impactful changes and trends shaping clinical study protocols globally. The session will also explore how vendor and partner relationships have adapted to these changes, highlighting key considerations for onboarding eClinical technology vendors and maintaining trust in these partnerships. A discussion between industry experts will further elaborate on these topics, providing diverse viewpoints and practical strategies for navigating the evolving clinical trial environment.

    Speakers

    Carla Reis
    Vice President of Accounts, 4G Clinical
    Chris Greenberg
    Senior Director, CTSM Systems and Analytics, 4G Clinical

    12 PM

    Challenges in clinical supply chain through the story of a clinical study

    • Supply planning and learnings from an ongoing clinical study
    • Identifying and managing in advance, factors that have the greatest impact to the study supply requirements
    • Planning and managing supply chain uncertainty arising from rapid and unforeseen challenges, such as: regional regulation changes, natural disasters and geo-political conflict

    Speakers

    Christina Paleopanidis
    Director, Global Clinical Supply Chain, Incyte

    12:30 PM

    Comprehensive clinical trial supply chain management: ensuring efficiency, compliance and success

    Clinical trial supply plays an essential role in the conduct of clinical trials, often involving significant complexity and expense. Effectively managing risk in complex studies, along with developing strategies to optimize savings and value, is crucial. CSI will outline strategies for the successful execution of even the most complex adaptive trials.

    Speakers

    Vanessa Dekou
    Managing Director, CSI

    1 PM

    Lunch and networking

    2:15 PM

    Sourcing vendors and partners for your clinical supply chain: what are the most important considerations?

    • Balancing cost alongside other considerations when selecting vendors
    • Key factors to consider when choosing vendors and partners in clinical supply
    • Advantages and disadvantages of choosing large vs small vendors
    • Working with international partners: additional challenges and how to address these

    Speakers

    Laurie Taraborrelli
    Clinical Programs and Compliance Specialist, Fujirebio Diagnostics

    2:45 PM

    Through the sponsors eyes: providing innovative clinical supply services through a sponsor-centric approach

    • Leveraging the power of people, experiences and technology to deliver results
    • Speed, flexibility, reliability, quality, cost: your clinical supply chain can have it all
    • Examples of innovative approaches that provide more efficient alternatives to traditional processes
    • Exploring technologies that can be used to reduce cycle time and cost

    Speakers

    Rocco Barone
    Senior Vice President, Clinical Supply Management, Clinigen
    Randa Atiyeh
    Vice President, CSM Client Services, Clinigen

    3:15 PM

    Afternoon refreshments and networking

    3:50 PM

    EXHIBITION APPLE PRIZE DRAW

    Visit our exhibitors’ booths throughout the day and collect stamps in order to enter our Prize Draw and be in for a chance of winning Apple devices or Amazon vouchers. The Prize Draw will take place in the Exhibition Hall. Make sure you don’t miss out!

    4 PM

    PANEL: Opportunities for innovation in clinical supply chains: what is on the horizon?

    • Emerging trends and technologies for clinical supply chains in the US: what’s new in 2024?
    • Exploring the potential of blockchain, IoT, and other digital technologies to revolutionize clinical supply chains
    • Automation in supply chains: how can this streamline processes and reduce human error
    • How IRT systems can optimize clinical supplies, improving efficiency and accuracy
    • An overview of new tools and solutions available on the market

     

    Speakers

    Jennifer Wittman
    Associate Director, Global Clinical Supplies Project Manager, Merck
    Paul Hingst
    Supply Chain Consultant, Crinetics Pharmaceuticals
    Seif M Oduor
    Senior Manager, CMC, Clinical Trial Supplies, Crinetics
    Carla Reis
    Vice President of Accounts, 4G Clinical

    4:30 PM

    Operational agility and maintaining flexibility in clinical supply chains

    • Highlighting an example of strategic execution of supply pooling across 6 global phase 3 studies.
    • Building collaborative partnerships with distribution vendors and IRT providers to ensure the agility of your clinical supply chain
    • Discussing the importance of making rapid adjustments to evolving trial parameters, country footprints, and enrollment
    • Examining methods to adapt logistics operations based on regulatory requirements and unforeseen circumstances

    Speakers

    Chris Campbell
    Associate Director, Clinical Drug Supply and Logistics, REGENERON

    5 PM

    Chairperson’s closing remarks

    Speakers

    Amanda Murphy
    Senior Director, Data Intelligence & Solutions, GlobalData

    5:05 PM

    NETWORKING DRINKS RECEPTION

    Streams

    Stream one

    Clinical Supply Logistics and Operations

    Stream two

    Clinical Supply Technology and Innovation

    9 AM

    PANEL: Sustainability in temperature controlled logistics: ensuring you minimize your carbon footprint

    • • Making environmentally conscious choices when selecting packaging materials: what options are available and which are the most sustainable?
    • • Pros and cons of active and passive containers when it comes to sustainability
    • • Methods of lowering the carbon footprint of temperature supply chains beyond just packaging
    • • Balancing cost, quality and sustainability in temperature controlled supply chains
    • • How can your temperature related operations contribute to meeting both internal and external sustainability targets?

    Speakers

    Luiz Alberto Barberini
    Head of External Manufacturing, Latin America, Bayer
    Ellyn Ensby
    Manager, Temperature Management and Control, Clinical Supply Chain, Janssen

    9:45 AM

    Optimizing cold chain logistics and improving green credentials to ensure the integrity of your products end-to-end

    • Latest technological advances and innovative systems adopted by the industry to enhance cold chain distribution: what should be on your radar?
    • Sustainability: aligning market growth with responsible practices to ensure businesses are making smarter decisions
    • Efficiently and effectively outsourcing management of temperature-sensitive materials to ensure your cold chain is never compromised
    • Expanding capacity on cold chain resources and enhancing end-to-end management to keep up with increasing demand and limited supplies

    Speakers

    Luiz Barberini
    Head of External Manufacturing, Latin America, Bayer

    10:15 AM

    Morning refreshments and networking

    11 AM

    CASE STUDY: Innovations in real time monitoring for temperature controlled clinical supply chains

    • An overview of solutions available for real time monitoring: pros and cons of different methods
    • Successfully integrating real time monitoring equipment while remaining cost-conscious
    • Risks and limitations of processes for monitoring temperature: how to mitigate against this to avoid temperature excursions and product waste

    Speakers

    Ellyn Ensby
    Manager, Temperature Management and Control, Clinical Supply Chain, Janssen
    Kristin Corcoran
    Temperature Management and Control Lead, Janssen

    8 AM

    Registration and refreshments

    9 AM

    PANEL: Considerations and best practice for working effectively with vendors and partners

    • The importance of integrated systems with CMOs: how much integration is useful?
    • Considerations when choosing technology partners in order to facilitate a strong partnership
    • Balancing degree of oversight over vendors and partners: how involved should you be?
    • Designing your vendor strategy: is it beneficial to work with multiple vendors or with one single partner?

    Speakers

    Laurie Taraborrelli
    Clinical Programs and Compliance Specialist, Fujirebio Diagnostics
    Reid Tonik
    Senior Director, Clinical Supply Chain, Eikon Therapeutics
    Paul Hingst
    Supply Chain Consultant, Crinetics Pharmaceuticals
    Joerg Wania
    Head of Clinical Trial Supply and Export Sales, STADAPHARM GmbH
    Bob Amareld
    Head of Quality and Supply Operations, Imugene

    9:45 AM

    Patient centricity in clinical trial supply chains: where could biopharma do more to support patients?

    • Ensuring timely delivery of trial medications to patients: options such as DTP and flexible scheduling
    • Avoiding one size fits all: exploring methods for gathering insights into patient preferences regarding medication packaging, delivery methods and scheduling
    • Exploring initiatives to involve patients in decision-making processes and clinical trial supply chain design

    Speakers

    Ram Raju
    Senior Vice President and Community Health Investment Officer, Northwell Health

    10:15 AM

    Morning refreshments and networking

    11 AM

    Breaking down silos in the clinical supply chain: how transparency supports robust and efficient planning

    • Promoting open communication channels for timely information sharing
    • Aligning goals and timelines to optimize resource allocation
    • Utilizing digital tools for real-time data sharing and visibility
    • Fostering a culture of collaboration and mutual support
    • Implementing consistent metrics and reporting standards for continuous improvement

    Speakers

    George Cortez
    Director, Clinical Supplies, on assignment at Endo

    11:30 AM

    CASE STUDY: IMP supply to EU countries under EU-CTR

    • The impact of the European CTR on IMP supply
    • Bridging the gap between CTD and CTR: what you need to know and how to navigate this
    • Challenges around labeling and ensuring your labels meet CTR requirements

    Speakers

    Yosuke Ito
    Manager, Program Management, Research and Development, NS Pharma

    12 PM

    Lunch and networking

    1:15 PM

    Navigating multiple regulatory agencies to help expedite supply chain times

    • Understanding the requirement and options for declaring biological materials to U.S. Customs and Border Protection (CBP)
    • Review of key U.S. regulatory agency authorities, such as CDC, FDA, USDA, and CBP
    • Discovering the latest non-compliant shipment issues for biological materials and pharma products and tips to avoid them
    • Learning about valuable resources and contacts for assistance

    Speakers

    Elliot N. Ortiz
    Chief Agriculture Specialist, Area Port of Philadelphia, US Customs and Border Protection

    1:45 PM

    Exploring expected trends with clinical supply chain needs from CDMOs

    • Emerging demands, flexibility and scalability in clinical supply chains
    • Integration of advanced technologies: AI, machine learning, and IoT for better tracking and efficiency
    • Assessing opportunities for incorporating sustainability practices and reducing carbon footprint
    • Enhanced collaboration and fostering stronger partnerships between sponsors and CDMOs
    • Data-driven decision-making: utilizing big data analytics for supply chain optimization

    Speakers

    Katarina Zahedi
    Analyst, GlobalData Healthcare

    2:15 PM

    Afternoon refreshments and networking

    2:40 PM

    EXHIBITION APPLE PRIZE DRAW

    Visit our exhibitors’ booths throughout the day and collect stamps in order to enter our Prize Draw and be in for a chance of winning Apple devices or Amazon vouchers. The Prize Draw will take place in the Exhibition Hall. Make sure you don’t miss out!

    2:45 PM

    SPEAKER HOSTED ROUNDTABLE DISCUSSIONS

    Interactive roundtable sessions offer a unique opportunity to come together with your peers to share best practice and develop solutions to critical challenges facing the clinical supply chain industry as a whole. Hosted by industry experts and each focused on a single issue, roundtables are an exciting, interactive way to build your personal network and learn from the experience and expertise of others.

    ROUNDTABLE 1: Importing and exporting biological materials to or from the U.S
    Elliot N. Ortiz, Chief Agriculture Specialist, Area Port of Philadelphia, U.S. Customs and Border Protection

    ROUNDTABLE 2: Handling vendor relationships in clinical trial supply chains
    Luiz Barberini, Head of External Manufacturing, Latin America, Bayer

    ROUNDTABLE 3: Just in time labeling: pros and cons for your trial
    Chris Campbell, Associate Director, Clinical Drug Supply and Logistics, REGENERON

    Speakers

    Elliot N. Ortiz
    Chief Agriculture Specialist, Area Port of Philadelphia, US Customs and Border Protection
    Luiz Barberini
    Head of External Manufacturing, Latin America, Bayer
    Chris Campbell
    Associate Director, Clinical Drug Supply and Logistics, REGENERON

    3:45 PM

    End of Conference

    Speakers

    Select a speaker to learn more

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    Ian Hoban
    Business Development Director, Abacus Medicine

    Ian has over 30 years of pharmaceutical industry experience, predominantly within global organisations such as Pfizer and Eli Lilly.  He built his reputation in the commercialisation of numerous brands in a variety of disease areas, and at every stage of the product lifecycle.

    During his career, Ian has worked closely with supply chain, ensuring accurate forecasting, and getting medicines to patients through the implementation of novel approaches.

    Before joining Abacus Medicine Pharma Services Ian worked in senior roles at two leading global clinical solutions companies.  He provided many leading pharmaceutical and biotechnology companies with successful comparator sourcing solutions which helped successfully deliver their pivotal late phase clinical trials.

    Session Details:

    Implementing sustainable sourcing practices for commercial medicines in your clinical trials

    2024-11-05, 11:30 AM

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    Lucy Fox
    Business Development Director, Abacus Medicine
    • 11 years clinical trial service experience
    • Worked closely with multinational pharmaceutical, virtual and biotechnology companies to define their clinical trial requirements. Acting as a consultant on technical aspects
    • Experienced in the management of IVRS technology for clinical trials
    • Worked closely with drug supply managers to effectively manage global supplies including forecasting and procurement from phase I to extensive phase III trials
    • Can develop creative solutions to fulfill customer needs
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    Bannikuppe Shivanna
    Director, Quality Control

    Biopharmaceutical professional of over 20 years with demonstrated capability across broad areas of CMC functions, specialized in cGMP analytical methods, technology transfer and CRO/CSP management. Over 15+ years of QC and technical operations management including compliant labs, quality systems, robust stability program, global reference standard and critical reagent program. Expertise in bioanalysis of small molecule, protein, mAb, vaccine products and biomarker for PK/PD, release, stability and product characterization studies. CMC support for IND, NDA and BLA submissions. Expertise in cGMP method validation for product/process/equipment/facility and systems. Contributed to success of commercial programs of anthrax vaccine and Erbitux; multiple oncology mAb products including cancer immunotherapy product Keytruda®. Depth in diverse areas of structure-function and applied studies on proteins. Enterprise focused leader of high quality results and project deliverables with team work and collaboration. Strategic and motivational leader committed to build high-performance teams with mentoring and coaching. Thorough understanding of regulatory guidelines, operational excellence, continuous process and performance improvements. Detail oriented, adept in written, verbal and interpersonal communication, and business savvy public speaking. Creation and setting-up of new functional biophysical and immunochemistry labs.
    GOALS: Work for companies and organization engaged in innovation and problem solving in vast areas of pharmaceutical development for human needs.

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    Deirdre Casale
    Senior Director, Supply Chain, Alnylam Pharmaceuticals
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    Nirav Shah
    Director, Clinical Drug Supply & Logistics

    Pharmaceutical professional with 20 years experience in managing global clinical supply chain activities including strategic planning and forecasting of clinical supply budgets, FTE's, supply requirements and IRT development. Also responsible for managing and maintaining relationships with CRO's, distribution vendors, suppliers, and packaging vendors.

    Session Details:

    How to recruit, train, and retain talent for Supply Chain 4.0

    2024-11-05, 2:15 PM

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    HANEEN MAZAHREH-BOIVERT
    Sr. Director, Global Clinical Supply, Optinose

    Haneen Mazahreh-Boivert is a global clinical supply expert and end to end supply chain advocate.  Throughout her 15+ year career, she has worked and consulted for numerous companies of varying footprints.  Haneen has successfully established and led numerous clinical supply chains from forecasting and planning, to vendor selection and management, clinical manufacturing and global distribution, to site management and drug accountability.  Her mantra is the right supplies at the right place at the right time and focuses her knowledge of operational excellence, KPI improvement, and process optimization to achieve this goal and build efficiencies into her projects. 

    She is a graduate of the American University, Rowan University, and Yale University with BS. Chemical Engineering, MS. Chemical Engineering, and Certification of Executive Leadership respectively.  Haneen is active in the Global Clinical Supply circuit, has published several articles and regularly speaks at industry conferences.  She is also active in Women in Engineering groups.   

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    Vanessa Dekou
    Managing Director, CSI

    Vanessa is the MD of Clinical Services International (CSI) a leading provider of Clinical Trial Supplies to the Biopharmaceutical Industry. Vanessa started her career as a research associate at Scotland Yard. Subsequently she worked for leading CROs and with some of the largest biopharmaceutical and Biotechscompanies to provide innovative solutions. She has extensive experience in drug development from Preclinical to registration and commercialization strategies and has secured product registration for several orphans and first in class drugs. She has a PhD in Cardiovascular Genetics from UCL, an MBA from Cambridge and Masters in Market Access from University m University of Lyon.

    Session Details:

    Comprehensive clinical trial supply chain management: ensuring efficiency, compliance and success

    2024-11-05, 12:30 PM

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    Reid Tonik
    Senior Director, Clinical Supply Chain, Eikon Therapeutics

    Global clinical supply chain expert with over 20 years of industry experience and a proven track record of successfully managing multiple clinical trial programs and teams from initial design through study close-out. Experience includes a 2-year international assignment, team and budget management, and optimizing departmental productivity by identifying opportunities for greater efficiencies and quality.

    Session Details:

    PANEL: Considerations and best practice for working effectively with vendors and partners

    2024-11-06, 9:00 AM

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    George Cortez
    Director, Clinical Supplies, on assignment at Endo

    As Director and Principal Consultant, George leads the Clinical Supply Consulting (CSC) team, providing strategic planning support to customers and partners. With over two decades of clinical supply chain experience, his focus is on patient-centric innovation, fostering collaboration, and driving results.  George is currently on assignment at Endo USA leading their Clinical Supplies department.

    Prior to joining CSC, George held previous leadership positions at Almac Clinical Services, ICON, Janssen Biotech, and Merck & Co., where he served as subject matter expert in multiple areas within the global clinical supply chain. George has a proven track record of spearheading high-profile programs across diverse therapeutic areas in R&D, affirming his expertise as a clinical supplies leader.

    Session Details:

    Breaking down silos in the clinical supply chain: how transparency supports robust and efficient planning

    2024-11-06, 11:00 AM

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    Francesco Santo
    Associate Director Global Clinical Supply Chain, HUYABIO

    A highly experienced and passionate Clinical Supplies Project Manager, Francesco has dedicated the past 17 years to ensuring the seamless execution of clinical trials by optimizing supply chain operations. His deep commitment to this field is driven by a relentless pursuit of excellence in delivering life-saving treatments to patients worldwide.  Throughout his career, he has honed a diverse skill set, encompassing:

    • Strategic Supply Chain Management
    • Regulatory Compliance
    • Cross-Functional Collaboration
    • Risk Management
    • Innovative Problem-Solving

    Francesco’s dedication to the clinical supplies industry is rooted in a profound understanding of the critical role it plays in advancing medical research and improving patient outcomes. He is committed to continuing his journey in this field, always striving to contribute to the betterment of global health.

    Session Details:

    The current landscape for clinical supply chains in the US and globally

    2024-11-05, 9:00 AM

    Session Details:

    Optimizing comparator sourcing processes for your clinical trial

    2024-11-05, 11:00 AM

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    Laurie Taraborrelli
    Clinical Programs and Compliance Specialist, Fujirebio Diagnostics

    Session Details:

    The current landscape for clinical supply chains in the US and globally

    2024-11-05, 9:00 AM

    Session Details:

    PANEL: Considerations and best practice for working effectively with vendors and partners

    2024-11-06, 9:00 AM

    Session Details:

    Sourcing vendors and partners for your clinical supply chain: what are the most important considerations?

    2024-11-05, 2:15 PM

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    Ellyn Ensby
    Manager, Temperature Management and Control, Clinical Supply Chain, Janssen

    Ellyn Ensby is a self-proclaimed generalist, with roles and experiences across plan, source, make, and deliver functions, and through the varied lenses of commercial, R&D, pharmaceuticals and consumer products.  She is a passionate people leader and is focused on evolving temperature management into a key capability and advantage for the Clinical Supply Chain.  Ellyn holds a B.S. in Interdisciplinary Engineering & Management from Clarkson University, and an MBA from DeSales University.  

    Session Details:

    CASE STUDY: Innovations in real time monitoring for temperature controlled clinical supply chains

    2024-11-06, 11:00 AM

    Session Details:

    PANEL: Sustainability in temperature controlled logistics: ensuring you minimize your carbon footprint

    2024-11-06, 9:00 AM

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    Kristin Corcoran
    Temperature Management and Control Lead, Janssen

    With an extensive background in pharmaceutical chemistry, Kristi brings a vast knowledge of product quality to the table. Utilizing her innovative strategic thinking and patient centricity, she focuses on delivering projects with emphasis on improving quality within the Clinical Supply Chain. Kristi holds a BS in Chemistry from Delaware Valley University, a Masters in Analytical Pharmaceutical Chemistry from The Illinois Institute of Technology, and several industry certifications.

    Session Details:

    CASE STUDY: Innovations in real time monitoring for temperature controlled clinical supply chains

    2024-11-06, 11:00 AM

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    Jennifer Wittman
    Associate Director, Global Clinical Supplies Project Manager, Merck

    Jennifer is an accomplished Project Manager at Merck, dedicated to driving innovations that enhance clinical supply chain efficiency. With over 24 years in the pharmaceutical industry, she is an expert in clinical supplies planning and operations, business process integration, and data analytics.

    She brings a deep understanding of project planning from her extensive career with key roles in resource planning, supply operations, and production readiness, where she successfully led initiatives in production and supply chain logistics. Known for her ability to drive cost efficiencies and improve productivity, Jennifer ensures projects are delivered on time and within budget while delivering measurable benefits for the organization.

    Adept at synthesizing complex data, she leverages innovative technologies to inform decision-making and operational improvements. Jennifer's commitment to fostering cross-functional collaboration has established her as a trusted leader in clinical supply chain management.

    Session Details:

    CASE STUDY: The e-reader for clinical trial medication: a Digital Display Labeling (DDL) system to replace traditional paper labels and booklets in clinical trials

    2024-11-05, 12:00 PM

    Session Details:

    PANEL: Opportunities for innovation in clinical supply chains: what is on the horizon?

    2024-11-05, 4:00 PM

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    Ram Raju
    Senior Vice President and Community Health Investment Officer, Northwell Health

    Dr. Ram Raju has a distinguished career over 40 years as a healthcare provider, teacher, researcher and community organizer. In his role at Northwell Health, Dr. Raju set the strategic vision to improve population health by finding ways to meet the needs of its most vulnerable communities, by examining the existing programs aimed at improving the health system's response to the community's needs and working with local organizations to address them. Northwell Health is the largest healthcare provider in the state of New York, is a system with 23 hospitals and 830 outpatient facilities that sees 2 million people every year in the New York metro area and beyond.

    Session Details:

    Patient centricity in clinical trial supply chains: where could biopharma do more to support patients?

    2024-11-06, 9:45 AM

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    Yosuke Ito
    Manager, Program Management, Research and Development, NS Pharma

    Session Details:

    CASE STUDY: IMP supply to EU countries under EU-CTR

    2024-11-06, 11:30 AM

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    Chris Campbell
    Associate Director, Clinical Drug Supply and Logistics, REGENERON

    Session Details:

    The current landscape for clinical supply chains in the US and globally

    2024-11-05, 9:00 AM

    Session Details:

    SPEAKER HOSTED ROUNDTABLE DISCUSSIONS

    2024-11-06, 2:45 PM

    Session Details:

    Operational agility and maintaining flexibility in clinical supply chains

    2024-11-05, 4:30 PM

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    Paul Larochelle
    Director, Global Clinical Supply Chain, Takeda

    Paul is an experienced, motivated, and enthusiastic professional/pharmacist specializing in the area of Clinical Supplies/Investigational Product Management. He aspires to make an impact on patient lives by motivating, inspiring, guiding, and mentoring teams to see the value of the work that they do and the contribution it makes to the lives of the patients we serve globally. With over 15 years of training and experience in this area, he has served in a multitude of roles, including study supply management, asset management (DS/API/DP Management), management and oversight of a secondary packaging operations team, site and resource planning, and development of multiple custom systems and tools to enable staff to work more efficiently and distribute information more readily.

    Session Details:

    CASE STUDY: Development and training initiatives: considerations for supply chain teams

    2024-11-05, 2:45 PM

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    Elliot N. Ortiz
    Chief Agriculture Specialist, Area Port of Philadelphia, US Customs and Border Protection

    Elliot Ortiz is a Chief CBP Agriculture Specialist with U.S. Customs and Border Protection (CBP), Office of Field Operations (OFO) in the Area Port of Philadelphia.  Mr. Ortiz began his career in December 2000 in the Port of Mayaguez, Puerto Rico.  Mr. Ortiz has more than 22 years of public service with CBP, and has worked in a variety of environments, including on the pre-clearance, maritime, air passenger, and cargo locations.  He has also been able to assist in several past domestic and international CBP events.

    Session Details:

    SPEAKER HOSTED ROUNDTABLE DISCUSSIONS

    2024-11-06, 2:45 PM

    Session Details:

    Navigating multiple regulatory agencies to help expedite supply chain times

    2024-11-06, 1:15 PM

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    Mary Zhang
    National Account Manager, US Customs and Border Protection

    Mary Zhang – National Account Manager since 2009, at the Center of Excellence and Expertise for the Pharmaceuticals, Health and Chemicals (PHC-CEE) with U.S Customs and Border Protection (CBP). Ms. Zhang's previous experience includes serving as a Senior Import Specialist for the Trade Operations Division in the Port of New York/Newark, and Chicago. Previously she worked for the Revenue Management at the United Airlines.

    Session Details:

    Optimizing clinical trial supply chain efficiency through CTPAT/Trade Compliance

    2024-11-05, 12:30 PM

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    Maxime Derep
    Director of Solutions Engineering, N-SIDE

    Maxime is an optimist and is passionate about problem solving. He is a Senior Consultant and has been working at N-SIDE for over 4 years. He supports pharma parters with the optimization of multiple trials and programs from different therapeutics area. He also helps those partners to understand the value of risk-based optimization and drive changes within their organizations. He loves to exchange ideas and discuss with people from the industry. Maxime has a Master in Business Engineering with a focus on supply chain.

    Session Details:

    PANEL: Incorporating artificial intelligence and machine learning into clinical supply chains

    2024-11-05, 11:00 AM

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    Amanda Murphy
    Senior Director, Data Intelligence & Solutions, GlobalData

    Amanda Murphy is the Director of Product Management at GlobalData, a company that focuses on research, data analytics and consulting that provide actionable insight into the pharmaceutical and medical device sectors.  She has 10+ years of experience working in pharmaceutical data science and web platform development (including BioPharm Insight, Lead Sheet, and the Pharma Intelligence Center).  She has developed models and solutions to support Clinical Operations & Feasibility teams plan and optimize trials, including an e-feasibility questionnaire tool resulting in 4x faster response rates from sites.  Amanda also has many years of experience supporting business development at CROs through data-driven lead delivery and CRM integration solutions.

    Session Details:

    Chairperson’s opening remarks

    2024-11-05, 8:55 AM

    Session Details:

    The current landscape for clinical supply chains in the US and globally

    2024-11-05, 9:00 AM

    Session Details:

    Chairperson’s closing remarks

    2024-11-05, 5:00 PM

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    Katarina Zahedi
    Analyst, GlobalData Healthcare

    Session Details:

    Exploring expected trends with clinical supply chain needs from CDMOs

    2024-11-06, 1:45 PM

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    Christina Paleopanidis
    Director, Global Clinical Supply Chain, Incyte

    Christina has over 20 years experience in Pharma holding various positions within Clinical Operations, Medical Affairs, Project Management, and the last 5 years in Global Clinical Supply Chain.

    Throughout the course of her career, she has provided support across all phases of Sponsor Clinical Studies at Incyte, GSK, Bristol Myers Squibb, and Gilead Sciences, as well as management of Expanded Access Programs and Investigator initiated trials.

    She currently holds the position of Director, Global Clinical Supply Chain at Incyte, with a focus in patient-centric forecasting, strategic planning, and distribution of drug supply for Incyte's portfolio.

    Session Details:

    Challenges in clinical supply chain through the story of a clinical study

    2024-11-05, 12:00 PM

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    Joshua Anderson
    Associate Director, Logistics Strategy, Clinical Supply Chain, Johnson & Johnson Innovative Medicine
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    Rocco Barone
    Senior Vice President, Clinical Supply Management, Clinigen

    Rocco joined Clinigen in 2022 to spearhead the Clinigen Clinical Supplies Management (CCSM) business unit.  His background of 20+ years in clinical supply along with his passion for operational excellence and continuous improvement have helped transform CCSM into an industry leading provider of clinical services.

    Prior to his time at Clinigen, Rocco spent 18 years in the clinical supply division at Merck & Co., Inc. His last position, before joining Clinigen in 2022, was Director and Site Head of Merck US Clinical Supply Operations.

    Rocco holds a Bachelor’s in Chemistry and a Master’s in Business from Moravian University.

    Session Details:

    Through the sponsors eyes: providing innovative clinical supply services through a sponsor-centric approach

    2024-11-05, 2:45 PM

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    Randa Atiyeh
    Vice President, CSM Client Services, Clinigen

    Randa is a proven leader committed to building high-performing teams and robust processes to deliver exceptional service.  She has over 20+ years as sponsor and vendor in the clinical supply industry making her an expert in the end-to-end supply chain.

    Her areas of expertise are Forecasting & Planning, Supply Planning, Project Management, Comparator Sourcing, Demand & Supply Balancing, Business Analytics, System Implementation and Continuous Improvement.

    Randa joined Clinigen in 2022 and has global oversight of the Project Management team and Proposals & Contract Management.

    Prior to her time at Clinigen, Randa was at Merck & Co. in various roles focused in clinical supply.

    Randa holds a Bachelor’s in Commerce and Engineering from Drexel University.

    Session Details:

    Through the sponsors eyes: providing innovative clinical supply services through a sponsor-centric approach

    2024-11-05, 2:45 PM

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    Paul Hingst
    Supply Chain Consultant, Crinetics Pharmaceuticals

    Paul is an experienced Clinical Supply Chain Professional with a 25-year career in the BioPharmaceutical industry.  His extensive career includes roles at major companies like Amgen and Thermo Fisher Scientific, where he honed his skills and made a significant impact.  He has served in varied roles from basic research and contract manufacturing to client services and account management.  He is a Principal Consultant and Co-Founder of Beacon BioPharm Associates, a clinical supply chain consulting firm, providing variable staffing solutions to small and mid-sized BioPharm clients.  Paul is an industry veteran and respected leader known for his expertise in clinical supply chain.

    Session Details:

    PANEL: Incorporating artificial intelligence and machine learning into clinical supply chains

    2024-11-05, 11:00 AM

    Session Details:

    PANEL: Considerations and best practice for working effectively with vendors and partners

    2024-11-06, 9:00 AM

    Session Details:

    PANEL: Opportunities for innovation in clinical supply chains: what is on the horizon?

    2024-11-05, 4:00 PM

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    Victoria Vargo
    Director, Clinical Supply, Karyopharm Therapeutics
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    Robbie Hill
    Director, Business Development, Mercalis

    Session Details:

    Aligning clinical supply strategies with sustainability goals

    2024-11-05, 9:30 AM

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    Tom Gottschalk
    Vice President, Business Development, Mercalis

    Tom has worked in the life sciences industry for over 26 years, with the first 10 as a pharmaceutical representative and marketing product manager for Bertek, Merck and GSK.

    Tom joined Mercalis 16 years ago, created the RxStudy Card offering in 2009 and for the past 14 years has been focused on changing the paradigm of the traditional clinical trial supply process to one of greater efficiency through the RxStudy Card.

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    Pauline Deplasse
    Head of Marketing and Strategy, N-SIDE

    Pauline has over 7 years of dedicated experience in clinical supply optimization, working with more than 30 sponsor companies of all sizes. She specializes in enhancing supply chain resilience and efficiency through advanced forecasting and planning techniques. Her work integrates technology and data to streamline processes, reduce environmental impact, and boost overall efficiency.

    Session Details:

    CASE STUDY: A journey to achieving end-to-end clinical supply chain optimization

    2024-11-05, 10:00 AM

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    Isaac Greenslade
    Director, Head of Demand and Supply Innovation and Transformation, Sanofi

    Isaac Greenslade has over 18 years of experience in clinical supply chain, clinical development, and CMC project management. He is currently the Head of Demand and Supply Innovation and Transformation at Sanofi, where he drives strategic initiatives to enhance operational efficiency, foster innovation, and optimize supply chain planning across the R&D organization.

    Session Details:

    CASE STUDY: A journey to achieving end-to-end clinical supply chain optimization

    2024-11-05, 10:00 AM

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    Sydney Reynolds
    Postdoctoral Fellow - Global Clinical Supply Chain, Takeda

    Sydney Reynolds, PharmD, MS, is the First Year Global Clinical Supply Chain Fellow at Takeda. Sydney graduated in May of 2023 from The Ohio State University College of Pharmacy with her PharmD and MS in Translational Pharmacology specializing in Clinical Pharmacology and Clinical Trial Design. Before that, she received her BS in Chemistry and Biology from the University of Indianapolis. Throughout pharmacy school, she was a Clinical Pharmacy Intern at The OSU James Cancer Hospital, where she was also heavily involved in research. She held leadership positions in Student College of Clinical Pharmacy (SCCP) and was a PharmD Ambassador for the college. For Sydney, pharmaceutical research is where her two passions collide – science and healthcare. She is excited to jumpstart her career with her fellowship and begin improving the lives of patients in the biopharmaceutical industry.

    Session Details:

    CASE STUDY: Development and training initiatives: considerations for supply chain teams

    2024-11-05, 2:45 PM

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    Jennifer Fenwick
    Senior Manager, Logistics and Distribution, Vertex Pharmaceuticals
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    Advisory Board

    Select a member to learn more

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    Chris Wallace
    Head of Distribution EMEA, Argenx

    Chris has over 35 years’ varied supply chain experience, having worked for several blue chip companies in a number of industries including 3rd party logistics services, automotive, medical device, nuclear fuels and biotech/pharmaceuticals.

    Originally from the UK but now based in Switzerland, he has been involved in life science - biotech/pharmaceuticals & medical device - for over 20 years of his career and has latterly been SVP Global Supply Chain at Clover Biopharmaceutical before last year moving to Argenx as Head of Distribution EMEA.

    He has developed, implemented and managed global healthcare supply chain strategies and operations on 6 continents. This has included different set-ups in multiple countries, including many in the Emerging Markets as well as the developed world.

    Chris has a degree in economics from Manchester University, an MBA from Aston University and a postgraduate diploma from London University. In his spare time, he plays golf badly and loves to sample great Italian food and red wines!

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    Luiz Barberini
    Head of External Manufacturing Latin America, Bayer
    • Over 25 years’ experience in Logistics, Supply Chain, Procurement and Demand Planning areas.
      Solid knowledge and experience in the whole S&OP process and its KPI´s inter-relationships with stakeholders
    • Demand Planning process management - pre-S&OP, with Sales, Marketing, Trade Marketing, Industrial Planning and Finance and customized tool design for such process
    • Management skills: experience with multidisciplinary and international teams (Brazil / Latin America / US).
    • Experience in S&OP, 3PL and Supply Chain Organization projects' implementation
    • Strong experience with Pharmaceutical and Consumer companies and Brazilian distribution model / 3PL contracts
    • Solid team management skills, as well as Customer Service relationship and management
    • Teacher for major Post Graduation Schools - Demand Planning and Procurement/Negotiation areas

    CSCP & CPIM APICS. Logistics & Supply Chain driven strategy. Distribution & Logistics, Demand Planning, S&OP, Procurement and Export experiences, focusing on Business necessities through effective leadership.

    Working as External Manufacturing Operations Manager Latin America at Bayer, in charge for external partners for CHC Division. Previously as Relationship Associated Director at Merck , Logistics Manager at Takeda/Nycomed Pharma, focusing on demand management, planning and distribution activities. Also has worked as Pfizer´s Logistic Manager and EFD´s Supply Chain Manager. Souza Cruz´s Procurement Manager and Rhodia's Logistic Supervisor.

    Specialties: Logistics, Supply Chain, Materials, Procurement , Services, Negotiation, 3PL contracts, S&OP, Demand Planning

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    Paul Hingst
    Supply Chain Consultant, Crinetics Pharmaceuticals

    Paul is an experienced Clinical Supply Chain Professional with a 25-year career in the BioPharmaceutical industry.  His extensive career includes roles at major companies like Amgen and Thermo Fisher Scientific, where he honed his skills and made a significant impact.  He has served in varied roles from basic research and contract manufacturing to client services and account management.  He is a Principal Consultant and Co-Founder of Beacon BioPharm Associates, a clinical supply chain consulting firm, providing variable staffing solutions to small and mid-sized BioPharm clients.  Paul is an industry veteran and respected leader known for his expertise in clinical supply chain.

    Session Details:

    PANEL: Incorporating artificial intelligence and machine learning into clinical supply chains

    2024-11-05, 11:00 AM

    Session Details:

    PANEL: Considerations and best practice for working effectively with vendors and partners

    2024-11-06, 9:00 AM

    Session Details:

    PANEL: Opportunities for innovation in clinical supply chains: what is on the horizon?

    2024-11-05, 4:00 PM

    View In Agenda
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    Francesco Santo
    Associate Director Global Clinical Supply Chain, HUYABIO

    A highly experienced and passionate Clinical Supplies Project Manager, Francesco has dedicated the past 17 years to ensuring the seamless execution of clinical trials by optimizing supply chain operations. His deep commitment to this field is driven by a relentless pursuit of excellence in delivering life-saving treatments to patients worldwide.  Throughout his career, he has honed a diverse skill set, encompassing:

    • Strategic Supply Chain Management
    • Regulatory Compliance
    • Cross-Functional Collaboration
    • Risk Management
    • Innovative Problem-Solving

    Francesco’s dedication to the clinical supplies industry is rooted in a profound understanding of the critical role it plays in advancing medical research and improving patient outcomes. He is committed to continuing his journey in this field, always striving to contribute to the betterment of global health.

    Session Details:

    The current landscape for clinical supply chains in the US and globally

    2024-11-05, 9:00 AM

    Session Details:

    Optimizing comparator sourcing processes for your clinical trial

    2024-11-05, 11:00 AM

    View In Agenda
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    Arnaud Dourlens
    Head of Clinical Trial Supply, Sanofi

    Arnaud Dourlens is an Arts et Métiers engineer, he began his industrial career in the FMCG sector where he held growing responsibilities. Then he joined the LVMH group where he reorganized new product launches and industrial investments in the Make-up segment in order to adapt to the need for innovation and time to market, thus providing a competitive advantage. He then managed the entire portfolio of industrial launches and investments in Perfumes, Skincare and Make-up for Parfums Christian Dior Group. During his career Arnaud held a wide variety of industrial roles. He joined Sanofi in 2017 as Production Director of a major solid oral form production site (>2.5 billion € turnover). He has been a key player in the development of the continuous improvement mindset and in the transformation of the site through IT projects, investments and activity growth following the acquisition of Boehringer Ingelheim consumer healthcare portfolio. Since the beginning of 2020, he’s been the global head of Sanofi Clinical Supply Chain Operations, managing worldwide clinical supply teams involved in more than 300 clinical studies.

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    Paul Larochelle
    Director Global Clinical Supply Chain Planning, Takeda

    Paul Larochelle has over 17 years of experience in a variety of positions within Clinical Supplies, including roles in clinical planning, production scheduling and planning, secondary packaging operations management, and business expert for a clinical inventory management system. Paul currently leads a team of Clinical Planning Leads at Takeda and is a member of the Global Clinical Supply Chain (GCSC) Leadership Team. He also oversees Takeda’s GCSC Post-PharmD Fellowship Program in partnership with the Massachusetts College of Pharmacy and Health Sciences (MCPHS). Paul’s prior organizations include Genzyme/Sanofi and Biogen, supporting therapies across all indications and stages of development.

    In addition to his primary responsibilities, Paul served as a coordinator of Pharmacy Industry Fellowships for the Genzyme/Sanofi MCPHS Fellowship Program (2009-2014) and precepted over 50 pharmacy students interested in a career in industry for several schools. He is currently the Chair of the Dean’s Advisory Board for MCPHS Boston School of Pharmacy and a member of the Pharmacy Advisory Board for Western New England University. He is also a member of the Clinical Trial Supply Conference Series Advisory Board.

    Paul completed a Post-PharmD Industry Fellowship in Clinical Research/Investigational Product Management with Genzyme/MCPHS, a Doctorate in Pharmacy from MCPHS, an MBA from Worcester Polytechnic Institute, and a degree in Biology from Providence College. Paul has also served previously as President of the Board of Directors for the Massachusetts Pharmacists Association (MPhA), and as President of the MCPHS Alumni Association.

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