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.
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.
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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Media Contact
Soumya Shashikumar, Xtalks, +1
(416) 977-6555 x371, skumar@xtalks.com, http://xtalks.com
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