14
DecemberSFDA workshop on quality variation in pharmaceutical products (Requirements and conditions)
Main building - Training and Conference Center
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» Objectives
During this workshop all relevant aspects regarding the quality assessment of post approval changes in pharmaceuticals will be discussed. You will get to know:
- Understanding the requirements of minor and major variations.
- Learn about some commonly encountered deficiencies and how to address them.
- The current guidance and risk assessment for nitrosamine impurities.
From Date |
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To Date |
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Workshop Type |
Public
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Presenting Language |
English
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The workshop is over