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PureFDA®: medical device consultants, device registration, Offices worldwide.
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QA/RA Consulting Group - FDA Quality & Regulatory Affairs for Medical Devices. Specializes in bringing new medical devices to market offering services including domestic and international regulatory affairs, design and development, quality management systems, auditing, and usability engineering.
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Explore Whitney Consulting's Free Resources Resource Materials Whitney Consulting is a regulatory consulting firm dedicated to the Chinese market. Since 1994, we have been providing international clients with services in Chinese medical device regulatory affairs, clinical affairs, and medical market research. From our offices in the United States and China, we bring clients up-to-date
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CE Marking, also referred as CE Mark is a legal requirement for medical devices (medical equipments) to market in the Europe. CE Marking (CE Mark) is recognized worldwide as a symbol of quality.
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Consulting Services for Medical Device Companies
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CMC MEDICAL DEVICES - YOUR QUALITYIS OUR SERVICE
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Compliance Insight is one of the most trusted FDA Regulatory Consultants offering Quality and Regulatory Consulting for Pharmaceutical, Medical Devices, Biologics & More.
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Medical Device Consultants offering ISO 13485 Quality Systems and Procedures and Medical Device Consulting Services
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Psephos Biomedica works with clients globally to bring innovative medical technologies to market by providing quality clinical, management and regulatory services.
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Full Service Medical Device CRO A single point of access for all your supporting Regulatory, Quality and Clinical Services Our Regulatory Services will guide you through the various (inter)national and local regulations to assure compliance and access for the particular market of interest. A sound quality
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Canadian Regulatory Affairs Consulting and Canadian Quality Assurance Services
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Regulatory affairs consultancy specialising in human and veterinary pharmaceuticals, pharmacovigilance and medical devices
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Learn more about Network Partners, a medical device and pharmaceutical consulting and contract staffing agency providing packaging engineering, regulatory affairs, labeling, cold chain solutions and project management.
Regulatory Expert Medical Devices
Niels Ole Andersen is a Regulatory Expert finding a pathway bringing Medical Devices to market with a pragmatic approach
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Homepage - Global Regulatory Partners, Inc.
About GRP 1 + Clients 1 + Projects 1 Offices World Wide What We Do We are a consulting company that provides a full spectrum of tailored Regulatory Affairs, Clinical, Quality and Pharmacovigilance Services to Pharmaceutical, Medical Device, Cosmetic, and Nutraceutical companies worldwide. Our main focus is to provide our life science clients with tailored … Homepage Read More »
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ORA Innovations: A leading provider of Medical Compliance Consulting Services for; Quality Management, Regulatory Affairs, Product Development, Product Licensing, and WH&S.
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Pharmaceutical and Medical Device Regulatory Affairs and Clinical Research Development Organisation
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Freyr provides regulatory services and solutions in India to comply with CDSCO regulations for pharmaceuticals, medical devices, cosmetics, and food supplements manufacturing companies.
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Regulatory Company, born in 2008 as a dedicated REACH consulting company, TEAM mastery now provides a range of services in Chemical Regulatory Affairs.
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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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Medical Device Consultants – Regulatory Affairs Specialist
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BIOREG Services - Regulatory Affairs for Startup Companies
BIOREG Services - regulatory affairs for medical device and medical products startup companies. We strive to develop your idea into an approved product.
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Asphalion: Regulatory Affairs and Life Science Consulting
Asphalion is an International Scientific and Regulatory Affairs consultancy that provides assistance in Pharmacovigilance, Submissions, RIM, CMC and more.
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TopPharm: Pharmaceutical regulatory affairs and regulatory consulting services in Poland and EU. We are former authority experts.
SRS | Scandinavian Regulatory Services
Regulatory and Quality consultancy company offering cervices for phamraceuticals, medical device, combination products, cosmetics and food supplements.
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Regulatory affairs consultants serving pharmaceutical and related industries in the Americas and globally. Specializing in regulatory compliance and business development for pharmaceuticals, medical devices, veterinary medicines, cosmetics, natural health products and related OTC wares.
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Veraque consulting. 我们满足您的需求
Veraque consulting provides regulatory affairs solutions in Mexico for medical devices and IVDs.
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QSE is organized to provide strategic and implementation services to the global medical device and diagnostics industry. Our business provides measurable quality systems and regulatory compliance solutions for virtually all of your business needs.
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