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Other links at Business Services > Consulting > Medical and Life Sciences > Regulatory Affairs |
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Q-NET LLC
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EU authorized representative service in accordance with the EU medical device directive and EU machinery directive. Also act as FDA US agent for foreign establishments.
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CATS Consultants
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EU regulatory affairs and preclinical/toxicological consulting.
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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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Pensa Technology Solutions Inc.
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21 cfr part 11 regulatory compliance of FDA pharmaceutical GMP validation for ERP life sciences computer information systems.
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Validation Technologies, Inc.
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Worldwide validation, quality, compliance, and production services for the medical device, pharmaceutical, nutraceutical, and biotechnology industries.
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