Archives: Agenda

• Why it is so important to have proper oversight over study conduct
• How to make it smooth and effective
• Which aspects of the trial should have your special attention
• How CRO can support with keeping oversight on the proper level

• Pre-selection through identification of CDMO exclusion criteria
• Finding synergies (for the process) through cooperation with academia and suitable grants
• The RfP- how to enable the comparison of apples with apples
• The ideal process and risk assessment

• Maximizing the opportunity for strategic input and design feedback from your CRO throughout the outsourcing process
• Overview of the typical areas where your CRO can guide and facilitate study optimization
• Examples of where CRO experience has transformed study design and operations, to sponsor advantage

• Overview of current air cargo professional programs focused on specialization of temperature-controlled air cargo management
• Insights into ongoing efforts to professionalize the industry across different regions
• How training programs are integrated into audit and certification programs to airfreight operators (airlines, ground handlers, freight forwarders etc)
• Difference between regulated and non-regulated training

• 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
• This session will present feedback from European pharma companies, offering a regional perspective on these trends and challenges. 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. An expert panel discussion will further elaborate on these topics, providing diverse viewpoints and practical strategies for navigating the evolving
  clinical trial environment.

• An eye in your dairy process and your effluent channels
• Reduce your product losses with multiwavelength sensor
• Improve your CIP cleaning performance
• Secure your product quality