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Understanding and Implementing USP : Analytical Instrument Qualification - Webinar

  • ID: 4871997
  • Webinar
  • February 2018
  • Region: Global
  • 90 Minutes
  • Compliance Online
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Why Should You Attend:

Analytical instruments should be qualified to demonstrate suitability for the intended use. Companies are unsure on what exactly to qualify or re-qualify, test and document. The main reason is that unlike fo\r analytical methods there was no clear standard with details for equipment qualification. This has changed. The USP has developed a chapter that provides a framework for analytical instrument qualification (AIQ).

This USP < 1058> webinar will give a good understanding of current and future FDA requirements and the USP framework. It also will provide detailed steps, examples and tools for cost-effective implementation.

Areas Covered in the Webinar:

FDA and EU requirements for analytical instrument qualification.
Most common inspection problems.
Terminology, scope and principles of the new USP chapter.
AIQ and its relation to method validation, system suitability testing and quality control checks.
Essential steps for AIQ: DQ, IQ, OQ, PQ
Purpose and contents of equipment qualification phases: design qualification, installation qualification, operational qualification, performance qualification.
Recommendations for firmware and software validation.
Roles and responsibilities: QA, manufacturer, user.
Approach for automated systems (incl. firmware/computer systems).
Requalification after equipment changes (move, repair, firmware upgrade, hardware upgrade).
Note: Product cover images may vary from those shown
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  • FDA and EU requirements for analytical instrument qualification.
  • Most common inspection problems.
  • Terminology, scope and principles of the new USP chapter.
  • AIQ and its relation to method validation, system suitability testing and quality control checks.
  • Essential steps for AIQ: DQ, IQ, OQ, PQ
  • Purpose and contents of equipment qualification phases: design qualification, installation qualification, operational qualification, performance qualification.
  • Recommendations for firmware and software validation.
  • Roles and responsibilities: QA, manufacturer, user.
  • Approach for automated systems (incl. firmware/computer systems).
  • Requalification after equipment changes (move, repair, firmware upgrade, hardware upgrade).
Note: Product cover images may vary from those shown
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Dr. Ludwig Huber, Ph.D., is the director of Labcompliance and editor of www.labcompliance.com, the global online resource for validation and compliance. Dr. Huber is the author of the books "Validation and Qualification in Analytical Laboratories" and "Validation of Computerized Analytical and Networked Systems". He has given multiple presentations mainly on GLP/GMP, 21 CFR Part 11 and Validation around the world. This included seminars, workshops and presentations for the US FDA, China SFDA, Korea MFDS, Singapore HSA, ISPE, Japan PDA, PIC/S and several other national health care agencies.
Note: Product cover images may vary from those shown
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