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    Webinar on October 2016 Validation Planning and Documentation

    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 Twitter Follow us – https://twitter.com/compliance4all Facebook Like us – https://www.facebook.com/Compliance4all