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Top > Consulting > Medical and Life Sciences > Regulatory Affairs
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European-based, Good Manufacturing Practice (GMP) Online Consultancy
Date Added: Aug 5, 2008 Hits: Rating: 0.00 Votes: 0
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MDTc is an independent consultancy to the medical devices industry. Based near Cambridge, England, MDTc helps bring products to market and comply with regulatory requirements.
Date Added: Aug 5, 2008 Hits: Rating: 0.00 Votes: 0
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RAA (regulatory affairs consultancy)
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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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Privately held virtual company in Encinitas, California, offering quality and risk assesments, remediation, IT system validation and training for FDA regulated industries.
Date Added: Aug 5, 2008 Hits: Rating: 0.00 Votes: 0
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Compliance for electronic record management for FDA regulated companies.
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Biotech Consultant LLC provides consulting services in the scientific and regulatory aspects of a wide range of medical devices and biologics with particular expertise in the areas of in vitro diagnostics (ELISA-based, PCR-based, SNPs, microarrays, pharmacogenomics, analyte specific reagent (ASR) regulatory compliance, and proteomics), medical device software (including bioinformatics), CPT coding reimbursement, and biotechnology-based products.
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Consultant and advocate for the medical device industry on issues of regulatory and standards compliance, risk management (ISO 14971) and general device safety.
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Consultant for medical device importers, manufacturers, and physicians intending to introduce medical devices into U.S. commerce. Expert witness for neurological devices.
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Providing a wide range of consulting services in GCP, GLP and GMP compliance.
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