In this free webinar, learn valuable insights into adapting clinical trial protocols to comply with new regulatory frameworks, specifically the International Conference on Harmonization Good Clinical Practice (ICH GCP) guidelines. Attendees will learn how sponsors and vendors can collaboratively leverage past experiences and lessons learned from previous studies to influence future clinical trial protocol implementation. The featured speakers will discuss the importance of effective communication, risk management and quality assurance within the sponsor–vendor partnership.
TORONTO, June 19, 2024 /PRNewswire-PRWeb/ -- This webinar explores the intricate dynamics between sponsors and vendors and how experience allows for adaptation based on past experiences and how best to support change based on new regulatory frameworks and changes to International Conference on Harmonization Good Clinical Practice (ICH GCP) guidelines.
In this webinar, the speakers will explore the collaborative approach possible and how both sponsors and vendors can leverage lessons learned on past studies to influence future clinical trial protocol implementation to achieve more successful outcomes.
When the pressure is on to reduce medicinal product wastage, decrease implementation time but not compromise on patient safety and data integrity, experience is key. The expert speakers will share insights on effective communication, risk management and quality assurance within the sponsor–vendor partnership.
The expert speakers will also delve into various facets of the sponsor–vendor relationship, emphasizing the development of trust to foster enhanced collaboration and leveraging vendor expertise to meet project requirements. They will address the influence of regulatory frameworks and offer strategies for adapting to new clinical trial protocols, as well as discuss the importance of protocol optimization by designing strategic endpoints.
Moreover, they will cover risk management and contingency planning by proactively identifying and mitigating risks, as well as the crucial roles of quality assurance and compliance in ensuring regulatory alignment and data integrity. Finally, the importance of effective communication strategies will be highlighted, underscoring their significance in successful project execution.
Register for this webinar to learn how you can adapt clinical trial protocols to new regulatory frameworks like the International Conference on Harmonization Good Clinical Practice (ICH GCP) guidelines and optimize protocol implementation to achieve successful outcomes.
Join Peter Craig, Senior RTSM coordinator, Novo Nordisk; Siobhan McKenna-Power, Principle Client Services Lead, 4G Clinical; and Libbi Rickenbacher (moderator), Sr. Director of Product Strategy and Partnerships, 4G Clinical, for the live webinar on Tuesday, July 09, 2024, at 10am EDT (3pm BST/UK).
For more information, or to register for this event, visit From Past to Future: Using Experience to Enhance Clinical Trial Protocols.
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