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From GlobalCompliancePanel
Software Verification and Validation Planning to Meet FDA Requirements - Webinar By GlobalCompliancePanel
The verification and validation of medical software is coming under increased scrutiny by the U. S. FDA.
Wednesday, October 19, 2011
10: 00 AM PDT | 01: 00 PM EDT
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Develop and Execute the Company Software VV Program - Webinar By GlobalCompliancePanel
Overview: The verification and validation of medical software is coming under increased scrutiny by the U. S. FDA.
This webinar will address the use of the FDA, GAMP, 21 CFR Part 11, "Electronic Records" / "Electronic Signatures", and other applicable industry software validation models, coupled with the ISO 14971 / ICH Q9 Product Risk Management models, to structure, run, and document
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