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Need EC Rep/UKRP for both EU-27 & UK? UK & EEA (EU/EC) European Authorised Representative/Authorized Representative (UK Responsible Person)
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medical device regulatory consulting, Full Service for your Quality, Regulatory, Auditing and Compliance Needs
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ToxinetConsult provides expert toxicological and regulatory consulting for pharmaceutical, medical device, food and cosmetic industries. Click to see more
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ArtPharm Ltd. – quality management, pharmacovigilance, regulatory and safety management of pharmaceutical products and medical devices..
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Oriel STAT A MATRIX has been a global leader in medical device quality and regulatory training, consulting and auditing since 1968.
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ISO 13485 Quality Systems | Medical Device Consultants
Medical Device Consultants offering ISO 13485 Quality Systems and Procedures and Medical Device Consulting Services
ATM Consulting Ltd. Website
The Quality Management and Regulatory Compliance Consultants
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Rephine Ltd. is a consultancy that provides a wide range of clinical and regulatory services to the pharmaceutical, medical device …
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Regulatory Navigation for Medical Devices
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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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WELCOME TO RAQA ApS Medical Device Regulation consultancy for manufacturers, distributors and importers REGULATORY AFFAIRS AND QUALITY ASSURANCE Read about our Regulatory Affairs and Quality Assurance services What you get at RAQA RAQA ApS started in 2018 to give Freelance and ad-hoc services to Medical Device Manufacturers, Distributors and Importers. RAQA has very service minded people who are good […]
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Training and webinars on regulatory affairs, regulatory compliance, quality assurance, risk and interim management in the pharmaceutical, food supplement and medical device industry.
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Weyergans High Care® AG
Your innovative expert for quality medical and cosmetic preparations and devices made in Germany.
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GMP Consultants & Outsourcing services, experts in EU regulations & Quality Management Systems servicing the pharmaceutical & medical device industries
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Operon Strategist - Medical Devices Quality Consulting Service, Medical Device Certification Consultant & Medical Devices Compliance Service Service Provider from Pimpri Chinchwad, Maharashtra, India
Regulatory Services in India, CDSCO, Regulatory affairs consulting
Freyr provides regulatory services and solutions in India to comply with CDSCO regulations for pharmaceuticals, medical devices, cosmetics, and food supplements manufacturing companies.
Medical Device Quality Management System (eQMS)
A medical device quality management system (eQMS) connecting quality and regulatory compliance with a human touch. ISO 13485:2016 Certified
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Medical Devices Consulting
MDC Engineers and Manager Regulatory Affairs provide medical-technical and regulatory knowledge. We consult, design and manufacture medical devices, in-vitro-diagnostic and laboratory equipment, which reflect the state-of-the-art and fulfill market-specific regulatory requirements.
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Medical Devices Consulting
MDC Engineers and Manager Regulatory Affairs provide medical-technical and regulatory knowledge. We consult, design and manufacture medical devices, in-vitro-diagnostic and laboratory equipment, which reflect the state-of-the-art and fulfill market-specific regulatory requirements.
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Jouhou Koukai - Japan market access
Consultants and consulting for regulatory affairs, auditing and training in the pharmaceuticals, biopharmaceuticals, medical devices, in-vitro diagnostics, biologicals, food, beverages, dietary supplements, nutraceuticals, cosmetics, veterinary medicine, healthcare, clinical trials, research, contract and outsoutcing, and life sciences industries
Arkin Consulting Group, LLC.
Regulatory affairs consulting FDA ISO medical device cGMP quality assurance control audit submission NDA 510(k) IDE clinical pharmaceutical registered agent compliance recall 483
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