Webinar: What is regulatory affairs?

February 16th, 8:30-9:30 CET

This webinar is intended for those who work within the life science sector and would like to gain a general understanding of regulatory affairs for human medicinal products.

Content: 

  • Regulatory affairs during development - opportunities and musts
  • Market authorization - building your dossier
  • Post-authorization – life cycle management

 

Presenter will be Erika Spens, Director of Regulatory Affairs at SDS Life Science.

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We will record the webinar. By attending, you agree that your name can be shown in the recording.

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