International Collaboration & Regional Updates
In the mist of global challenges and the implementation of flexibilities to accelerate patients’ access to medicines, collaboration is the key to advance. Different regulatory bodies from around the world will share updates related to their regional success stories and lessons learnt from the interactions with the various healthcare stakeholders.
Who is This Track Designed For?
This track is designed regional health authorities representatives, key industry leaders in these regions and all professionals interested in learning more about global regulatory processes.
Topic Leader
Sara Torgal
Senior Manager, Scientific Programmes
DIA, Switzerland
Key Topics
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Day 1: Tuesday, March 13th
Middle East Townhall: Future-Proofing the Regulatory Framework
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Day 2: Wednesday, March 13th
FDA Townhall -
Day 3: Thursday, March 14th, Gold Hall
DIA Europe 2023 Highlights
It will provide updates on key developments on the GCP Renovation (ICH E6, ICH E8), Clinical Trial Regulation, the Clinical Trial Information System, data submission, transparency, navigating ethical approval, study design in the digital age, innovative clinical trial designs (umbrella and platform trials, patient centricity), digital tools in development and other hot topics. It should be a must-attend for optimising development programmes and identifying cost savings through efficiency and innovation.