Understanding and Implementing USP : Analytical Instrument Qualification - FDA Webinar By Compliance (FDA)
Venue: Online Event
|Event Date/Time: Mar 22, 2011||End Date/Time: Mar 22, 2011|
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 for 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 Seminar:
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: Use this promocode(117660) for 10% discount.