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