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Cofactor Technologies provides international quality assurance and regulatory affairs consulting services to medical device companies worldwide.
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raPHARM is a consultancy and education office specialising in pharmaceutical and medical devices regulatory affairs.
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We live your needs Veraque consulting provides regulatory affairs solutions in different countries for medical devices and IVDs. We can help you with any step of your regulatory strategy. Contact us Just choose the country you are interested in Just choose the country you are […]
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Regulatory affairs consultancy specialising in human and veterinary pharmaceuticals, pharmacovigilance and medical devices
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CMC MEDICAL DEVICES - YOUR QUALITYIS OUR SERVICE
EC REP of Medical Devices, Consultant of CE mark, ISO 13485, OBL Agreements, Regulatory Affairs
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Acknowledge Regulatory Strategies specializes in Regulatory Affairs (RA) and Quality Assurance (QA) consulting exclusively for the medical device and In Vitro Diagnostic (IVD) industry. When you hire us, you also hire our entire network of current and former FDA reviewers, scientists, engineers, and
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Cosmereg regulatory affairs consultants assist clients to comply with the US FDA, Health Canada and EU regulations for cosmetics, food, medical devices and dietary supplements industries.
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Unitron Regulatory, expert in medical device regulation, life science consulting and product certification in the field of medical devices.
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Nilo Medical Consulting offers medical device and combination product consulting for FDA regulatory submissions such as 510(k), IDE, PMA, etc. We specialize in cardiovascular devices, dental devices, combination products, and pediatric device regulations.
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Operon Strategist is the best medical device consultant in India. Experts in Medical Device Quality Consulting and Regulatory services along with CDSCO, US FDA, CE, and Turnkey Projects.
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QAid provides consultancy on regulatory affairs (a.o. CE-marking), quality systems (ISO-13485), product development and project management to companies in the medical device and in vitro diagnostics industry.
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Regulatory affairs and technical consultancy services specialized in Mexican sanitary regulation of medical devices for obtaining health registry from COFEPRIS
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PDS is a pharmaceutical and regulatory consultancy serving the pharmaceutical, biopharmaceutical, medical device and cosmetic industries.
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MTC is a consultancy offering regulatory and clinical services to the medical device industry world-wide
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Raland Compliance Partners provides regulatory and compliance solutions in the pharmaceutical, biotech, and medical devices industries.
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Lachman Consultants provides FDA Compliance Consulting, Regulatory Affairs, Due Diligence Audits & Technical Services for Global Clients.
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