Facility Validation Web-based Seminars
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From GlobalCompliancePanel
Developing the Master VV Plan to Meet US FDA ISO 13485 and 14971 Requirements - Webinar By GlobalCompliancePanel
...from process / equipment V&V
* Process / Equipment / Facility Validation - FDA's new guidance
* When and How to use DQ, IQ, OQ, PQ, or their equivalents
* How to use Product Risk Management Tools (per ISO 14971 and ICH Q9)
* The 11 key documents for software validation
* Incorporating 21 CFR Part 11 requirements
* Suggested "test case" formats
Who will benefit:
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