Clinical Trial Supply New England 2020
The Westin Waltham
24th-25th March, 2020
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Clinical Trial Supply New England 2020
Following on from another successful conference Arena International will be returning with full force to Waltham in March to celebrate another edition of the Clinical Trial Supply show.
2020 will gather the key stakeholders in the clinical trials community, including the FDA, US Customs and Border Protection, Biogen, Sanofi, and Blueprint Medicines Corporation. With interactive session formats, fresh content and networking, the event will provide attendees with an unparalleled opportunity for collaboration between players across the whole industry.
We look forward to seeing you there!
WHAT TO EXPECT FOR 2020?
The Clinical Trial Supply series is a unique platform for clinical trial sponsors and solution providers. This event is aimed at enabling knowledge-sharing, benchmarking and network-building amongst biopharma industry peers.
200+
ATTENDEES
30+
EXHIBITORS
25+
SPEAKERS
65%
ATTENDEES AT
DIRECTOR+ LEVEL
Why Attend?
NETWORK
-

This is an exceptional networking opportunity for the clinical supply chain industry. Attendees will come from across the New England pharma hub and beyond to network and make new connections.
LEARN
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Each Clinical Trial Supply conference programme is written in collaboration with the local industry. Our production team will research with senior local leaders to devise an educational programme which meets the needs of that community.
ACTION
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The Clinical Trial Supply exhibition will feature leading solution providers and innovative disruptors to showcase the latest in supply chain management. Attendees will leave with new ideas and new contacts to solve common problems and capitalise on the opportunity that next generation technology offers.
Troy Petrillo
Supervisory Consumer Safety Officer,FDA
Biography:
Session Details: INTERACTIVE SESSION: Pick & Mix: Q&A with the FDA - regulation 25-03-2020, 8:30 am View In Agenda
Stephen King
Compliance Officer,FDA
Biography:
Session Details: INTERACTIVE SESSION: Pick & Mix: Q&A with the FDA - regulation 25-03-2020, 8:30 am View In Agenda
Sean Smith
Biological Threat Exclusion Coordinator,US Customs and Border Protection
Biography:
Session Details: KEYNOTE: How to ensure your clinical supplies pass US border control from the CBP perspective - logistics 24-03-2020, 8:30 am View In Agenda
Adam Pitt
Biological Threat Exclusion Coordinator,US Customs and Border Protection
Biography:
Session Details: KEYNOTE: How to ensure your clinical supplies pass US border control from the CBP perspective - logistics 24-03-2020, 8:30 am View In Agenda
Pavel Komůrka
Packaging Innovation – Sustainability Coordinator,Orkla ASA
Shell Lee
Associate Director, Supply Chain,Blueprint Medicines Corporation
Biography:
Session Details: Chairman’s Opening Remarks 24-03-2020, 8:20 am Updates in GS1 serialization clinical supply – packaging and labeling 24-03-2020, 9:30 am Connecting clinical and commercial supply chain – operational design 25-03-2020, 11:30 am View In Agenda
Tieming Ruan
Director of Combination Product,Kiniksa Pharmaceuticals
Biography:
Session Details: Advancements in combination products and how they fit into the supply chain – complex products 25-03-2020, 9:30 am View In Agenda
James Sherley, Director, Asymmetrex, LLC
Director,Asymmetrex, LLC
Biography: James L. Sherley, M.D., Ph.D. is the founder and director of Massachusetts stem cell biotechnology company Asymmetrex, LLC. Asymmetrex develops and markets technologies for advancing stem cell medicine, including the first-in-kind technology for specific counting of adult tissue stem cells. This technology is also applied to design optimized procedures for more effective manufacturing of therapeutic adult tissue stem cells at greatly reduced cost. Dr. Sherley is a graduate of Harvard College, with a B.A. degree in biology, and the Johns Hopkins University School of Medicine, earning joint M.D. and Ph.D. degrees. Prior to founding Asymmetrex, he held academic research appointments at the Fox Chase Cancer Center, Massachusetts Institute of Technology, and Boston Biomedical Research Institute. Dr. Sherley’s professional awards include Pew Biomedical Research Scholar, Ellison Medical Foundation Senior Scholar in Aging Research, and NIH Director’s Pioneer Award.
Session Details: Special challenges in supply and partner-sourcing for stem-gene clinical trials – vendor relations and procurement 24-03-2020, 1:30 pm PANEL DISCUSSION: How can we enhance the vendor-sponsor partnership to encourage scientific and technical innovating for smooth supply chain operations? – vendor relations 24-03-2020, 2:30 pm View In Agenda
Scott Sutton
Director Commercial and Clinical Supply Chain,Stealth Biotherapeutics
Biography:
Session Details: Updates in GS1 serialization clinical supply – packaging and labeling 24-03-2020, 9:30 am CASE STUDY: Innovation in supply-pooling models – new innovation 25-03-2020, 2:15 pm View In Agenda
Imran Shakur
Senior Manager, Clinical Planning and Operations,Biogen
Biography:
Session Details: Q&A SESSION: Capitalizing on Interactive Response Technology in Clinical Supply Management – tech and innovation 24-03-2020, 11:00 am FIRESIDE CHAT: Incorporating blockchain in clinical trial supply logistics – new innovation 25-03-2020, 1:45 pm View In Agenda
Rajni Aneja
Head of Digital Strategy/Transformation,Sanofi
Biography:
Session Details: The future of Direct-to-Patient trial supply – emerging models 24-03-2020, 3:30 pm View In Agenda
Lisa Kaufman
Associate Director, Quality, Process and Risk Management,AstraZeneca
Biography:
Session Details: Best practices for aligning clinical trial supply to adaptive design – operational design 25-03-2020, 12:00 pm Speaker Hosted Roundtables 25-03-2020, 3:15 pm View In Agenda
Kaitlin Bova
Clinical Quality Assurance Fellow,Novartis Institute for BioMedical Research (NIBR)
Biography:
Session Details: Speaker Hosted Roundtables 25-03-2020, 3:15 pm View In Agenda
Brenda McGrath
PhD, Associate Director Operations,inRegen
Biography:
Session Details: Global supply chain: managing an international clinical trial for autologous cell therapy.- emerging markets 24-03-2020, 4:00 pm View In Agenda
Janel Kelly
Clinical Supply Manager,Biogen
Biography:
Session Details: CASE STUDY: Are you prepared for an inspection? Lessons learned from a MHRA inspection - regulation 25-03-2020, 9:00 am View In Agenda
Matthew Leets
Associate, Logistics and Trade Compliance,AMAG Pharmaceuticals, Inc.
Biography:
Session Details: Logistics and Compliance 101: Importing international materials for US Clinical Trials - logistics 24-03-2020, 10:00 am View In Agenda
Eyal S. Ron
Ph.D. Board Member,AcuityBio Corp
Biography:
Session Details: Selecting a comparator sourcing model and the best vendor to implement it - procurement 24-03-2020, 2:00 pm PANEL DISCUSSION: How can we enhance the vendor-sponsor partnership to encourage scientific and technical innovating for smooth supply chain operations? – vendor relations 24-03-2020, 2:30 pm View In Agenda
Katie Bielat
Associate Clinical Supply Manager,Apellis Pharmaceuticals
Biography:
Session Details: Temperature control 101: How to best ship and store your IMPS – complex products 25-03-2020, 10:00 am View In Agenda
Amanda Murphy, Director of Product Management, GlobalData
Director of Product Management,GlobalData
Biography: 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: Planning for supply and storage during feasibility – operational design 25-03-2020, 11:00 am View In Agenda
Frank Leu
CEO,Novapeutics
Biography:
Frank Leu is a Co-Founder and CEO of Novapeutics at Philadelphia, PA - a biopharma spun-out from the University of Pennsylvania, developing a first-in-class small molecule beta-cell restoration curative for type 2 diabetes. Prior, Frank was at a specialty pharma Verto Institute, developing biologic therapeutics for treating the neuroendocrine cancer. Frank graduated with a Pharmacology Ph.D. from Weill Cornell Graduate School of Medical Sciences in 2001, and then post-doc in a Howard Hughes Medical Institute laboratory at the Rockefeller University in molecular enzymology. He has served as an adjunct instructor at the Rutgers Cancer Institute of NJ, and is an adjunct professor at the pharmacology department of the Thomas Jefferson Medical University. Frank also founded BioPharMatrix developing blockchain solutions to lifescience innovations at all phases, and serves as advisor to the Pennovations center working with 1776 / Benjamins Desk. Frank is a thought leader in the blockchain architecture innovations in the life-sciences and drug development, Frank serves on multiple advisory boards and frequently served as chairman, speaker, moderator, and facilitator for many life-sciences and drug development events.
Session Details: View In Agenda
Danny Lee, Associate Director
Associate Director,Atreca
Biography:
Session Details: Utilizing tools for demand planning and to forecast your supply – tech and innovation 24-03-2020, 12:00 pm View In Agenda
Sponsors
Catalent solves today’s clinical trial challenges and develop innovative solutions for the future. Catalent’s commitment to quality and service excellence is evident in its flexible solutions, modern global facilities, and over 25 years’ experience reliably supplying thousands of studies of all sizes and complexities around the world.
Xerimis
Industry: Healthcare,
SPONSORSHIP ENQUIRIES
To enquire about sponsorship opportunities for the Clinical Trial Supply series, please :
Paul Adams
Head of Sales – Health
T: +44 (0)20 7936 6948
E: Pauladams@arena-international.com
SPEAKER OPPORTUNITIES
The programme for the Clinical Trial Supply New England conference is underway. If you have a case study, or key message to deliver to this audience, please contact us below with your proposal.
Amy Malkani
Conference Producer
T: +44 (0) 161 359 5839
E: amy.malkani@arena-international.com
