Other links at Business Services > Consulting > Medical and Life Sciences > Regulatory Affairs |
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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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Perkins and Perkins
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FDA consultants Perkins and Perkins, Inc. conduct mock FDA audits to insure Good Clinical Practice (GCP) compliance, quality assurance and FDA audit preparation.
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Reg123.com
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Reg123.com is a portal for the new medicinal product development community with a focus on regulatory affairs and the pharmaceutical drug development process.
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