Event info
Date:09 Feb
Time:10-10:45
Venue:Online
Contact person

EXTERNAL EVENT

This is an external event. If you have any questions please follow the sign up link and contact the organizer.

The Importance of Regulatory CMC Strategy During Early Development

Accelerate development using a Quality Target Product Profile

Having the right Chemistry, Manufacturing, and Controls (CMC) documentation throughout drug development is essential for avoiding pitfalls, ensuring an efficient regulatory review process, and achieving the goals for your product. The key is an early development regulatory strategy that includes CMC.

Join LINK Medical Research regulatory CMC webinar to strengthen your knowledge of how regulatory CMC strategies can accelerate the drug development process and become familiar with strategic tools such as the Quality Target Product Profile (QTPP).

Date: Thursday 9th of February 2023
Time: 10:00 – 10:45 GMT
Venue: Online, Zoom

 

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Program 

10:00Start and introduction 
Hilde Holme
Product Development
Hilde Holme
Quality Target Product Profile
Marianne Ammitzbøll
CMC Documentation & Roadmap
Hilde Foros and Lone Dyrby
Summary
Lone Dyrby​
10:30Q&A
10:45End

 

 

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