Meetings/Workshops on Healthcare Technologies in Switzerland

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Lifecycle Management of Analytical Methods and Procedures - according to new FDA and USP guidelines
29 Apr 2020 - 30 Apr 2020 • Zurich, Switzerland
Organizer:
Complianceonline
Abstract:
Results of analytical methods are used as the basis for important decisions during development and manufacturing of pharmaceutical products. All regulatory agencies expect the regulated industry to have procedures in place to ensure suitable levels of reliability, accuracy and precision of such methods. The procedures should cover lifecycle phases from design, development, validation to on-going routine use.
Contact:
Phone: [18887172436];     Email: referral@complianceonline.com
Topics:
Computer System Validation seminar, USP <1058>, GAMP 5, equipment calibration, system validation, qualification and validation strategy, archive raw data from hybrid systems, Analytical Instrument Qualification, USP General Chapter <1058>, instrument qualification lifecycle, 21 CFR Part 211, Part 11, PIC/S, EU Annex 11, GMP Computer Systems, Laboratory Computerized Systems, Use of Excel in QC Laboratory, revalidation of chromatography, data security and integrity issues.
Event listing ID:
1329132


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Last updated: 11 February 2020