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SFDA workshop on quality variation in pharmaceutical products (Requirements and conditions)

Main building - Training and Conference Center

» 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.


        Registration Link

From Date
. 14-12-2022 . 11:00:00 am
To Date
. 14-12-2022 . 2:00:00 pm
Workshop Type
Presenting Language
The workshop is over