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Other links at Business Services > Consulting > Medical and Life Sciences > Regulatory Affairs |
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Cro.nu
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CRO in drug development process in close collaboration with the preclinical and clinical departments of pharmaceutical and biotech companies.
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Medical Device Consultants, Inc. (MDCI)
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provides worldwide regulatory, clinical, and quality assurance consulting services to medical device and diagnostic product manufacturers to meet US, Canadian, and European requirements.
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Horizon Phoenix Group-Medical Quality Consulting Firm
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Quality/regulatory consultants for medical device, pharmaceutical and biotechnology industries. Services include: CE Marking, Authorized European Representative, USFDA, 510ks, PMAs, US Agent and Canadian Licenses.
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Schell Associates
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Consulting services including regulatory affairs, preclinical and GLP testing, manufacturing, quality, compliance, and clinical studies.
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