RAPS European workshops provide insight into some of the most urgent and crucial issues facing regulators, manufacturers and regulatory professionals working with healthcare products for the European market. Here's what's next:
RA Considerations During Clinical Development in the EU
17 February
This workshop, hosted by @Adriaan Fruijtier, will provide an analysis of writing of a regulatory plan, emphasizing which key aspects to consider and exploring several pathways to expedite development.
Click here to learn more.
The EU Clinical Trial Regulation18 February@Adriaan Fruijtier is hosting this workshop too, and will discuss the new Regulation EU No 536/2014 and the many regulatory professionals need to know.
Learn more here.
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Ryan Connors
Community Engagement Coordinator
RAPS
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