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Other links at Business Services > Consulting > Medical and Life Sciences > Regulatory Affairs |
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Associates
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Associates. He is an electronics engineer and regulatory affairs executive with over thirty years experience in the medical device business, specializes in Good Manufacturing Practices auditing, consulting, and training.
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Validation and cGMP Compliance
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Equipment and Software Validation. Part 11 of 21 CFR Compliance. Regulations, cGMP, Validation knowledge base. FDA Warning letters.
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