Technical and regulatory requirements for developing a medicinal product are becoming stricter every day, the products themselves become more and more complex. This training will go through the key scientific points for the development and registration of your medicine, and provide a focus on US FDA and Europe expectations for CMC. This online training will covers general requirements for small molecules and biologics. #webinar
Key learnings:
Different Level Requirements
Overview of Challenges
Appropriate Specifications
Justify the Choice
Appropriate Specifications
Understand the Requirements
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