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Implemented in August 2008, USP General Chapter on Analytical Instrument Qualification (AIQ), has just been updated and the new general chapter is effective from August 2017. The evolution of this general chapter to clarify the requirements of the 4Q stages, particularly differences between OQ and PQ, and the inclusion of User Requirements and Software Validation is of global significance because the USP is the only Pharmacopeia that provides guidance on Analytical Instrument Qualification.

As an attendee, you will learn more about:

  • What the new USP general chapter contains
  • How to comply with the new requirements
  • Why companies need to update SOPs for AIQ now

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