Friday, March 10, 2023

Gain in-depth knowledge of Chemistry, Manufacturing and Controls (CMC)

1-Week To Go!

Greetings!


The objective of this course is to provide a strong understanding of the importance and underlying principles for CMC requirements from the regulatory perspective. Participants will gain an understanding of the CMC portion of a Common Technical Document (CTD) which is the format that regulatory submissions in Canada and the EU must be filed.

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Course Outline


The following specific topics will be addressed in detail:

  • Role of CMC in drug development
  • Nomenclature and characterization of drug substance
  • Analytical methods and validation
  • Manufacturing, in-process controls and process validation
  • Developing drug substance and drug product specifications
  • Stability, stability-indicating tests and how much change is acceptable
  • Regulatory expectations for product characterization
  • Drug Master Files
  • Structure, content and components relating to CMC section of a regulatory submission
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Date and Time:

March 17, 2023

9:00 AM - 5:00 PM (EST)


How is the webinar delivered?

OnlineLive, interactive, instructor-led

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Interested in this workshop?

Register today by calling our team at 416-502-2277 or email us at info@aaps.ca.

Academy of Applied Pharmaceutical Sciences

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