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Recorded Webinar – Chemistry, Manufacturing and Controls (CMC) Training

March 22 @ 8:00 am - 5:00 pm

Get Career-Ready in Ontario with AAPS!

Recorded Webinar – Chemistry, Manufacturing and Controls (CMC) Training

Recorded Webinar Time: 5 Hours Cost: CAD$300+HST (50% off of $600 – limited time only) Buy Now!

Abstract

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.

Course Outline

This course provides an in-depth analysis of the CMC portion of a Common Technical Document. 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

Who Should Attend

This one-day course is valuable for Directors, Managers, Supervisors, Associates in the Pharmaceutical, Biopharmaceutical, Vitamins, Herbals, Medical Devices and allied industries with daily responsibilities in the following areas:
  • Regulatory Affairs
  • Quality Assurance
  • Product Submission
  • Training
  • Consultants
  • Clinical Research
  • Documentation and Technical Writing
  • Project Management
  • Product Development
  • Others who interact together to launch a product

Details

Date:
March 22
Time:
8:00 am - 5:00 pm