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 plan, structure, run, and document acceptable software validations.
Who Will Benefit:
Senior management in Drugs, Devices, Combination Products, Biologics, Dietary Supplements
QA / RA
Software development, programming, documentation, testing teams
R&D
Engineering
Production
Operations
Consultants
Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com
http://www.compliance4all.com/
Event Link : http://bit.ly/2aVOwae
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