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Other links at Business Services > Consulting > Medical and Life Sciences > Regulatory Affairs |
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ERA Consulting Group
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Specialist services for pharmaceutical companies in regulatory affairs, including the development/registration of biotechnology and biological medicinal products, with offices in Europe and the United States.
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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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Global Regulatory
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Pharmaceutical, medical device, biotechnology, food, and nutraceutical consulting for the international markets.
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Solutions MDI, Inc.
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clinical affairs, quality systems, compliance strategies, CE mark and FDA submissions.
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European Authorized Representative
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Offers CE marking, US agent services to non-European medical devices manufacturers under AIMD, MDD, and IVD, under EU directives from Brussels, Belgium.
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