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Pharmaceutical and Regulatory consulting | Medical Devices
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Medical Device Regulatory Consultants & More | Cofactortech.com
Cofactor Technologies provides international quality assurance and regulatory affairs consulting services to medical device companies worldwide.
Korea medical device regulatory consulting
We provide regulatory supports for medical device registration in South Korea. Our services include medical device registration with the Korea health authorities, KGMP certification, Reimbursement coding with HIRA, In-country Representation and ad hoc services.
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Niels Ole Andersen is a Regulatory Expert finding a pathway bringing Medical Devices to market with a pragmatic approach
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ARQon is a medical device consultant for Regulatory, Quality RA/QA, device registration, clinical trials, ISO13485, GDPMD, MDSAP and distribution consulting.
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Paladin Medical®, Inc. offers a full range of medical device regulatory, clinical, and technical services for premarket applications and regulatory compliance.
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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FDA consulting for the medical device industry, pharmaceutical industry and food industry for US and EU FDA quality assurance and regulatory compliance and medical Device Reimbursement %
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Susanne Merk | Regulatory Medical Writing | Medical Devices
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Freelance consultant with +25 years of experience in medical devices, including sterile and / or implantable devices
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Best Medical Device Consultants in India | Operon Strategist
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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raPHARM regulatory affairs consulting and education
raPHARM is a consultancy and education office specialising in pharmaceutical and medical devices regulatory affairs.
International Medical Device Regulators Forum
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Pharmaceutical and Medical Device Regulatory Affairs and Clinical Research Development Organisation
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Regulatory Affairs Consultants Ireland, Pharmaceutical Regulatory Compliance Service
EMRC, Regulatory Affairs, Pharmaceutical, Consultancy, Advice, Medical Device, Registration, CE Marking , Wholesale Services
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I3CGlobal (IN) is one of the most popular medical device consultants firm by accelerates documentation preparation times and helps customers achieve early certifications through digital technologies and an experienced workforce, all with economical pricing.
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Medical devices
China Medical Device is online Medical Device database of China Medical Devices and China Medical Device Suppliers.
Medical Device Quality Management System | LuminLogic Software
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DM2TC homepage - Medical devices technical consulting
DM2TC provides advice and know-how to help medical devices industries and startups through the steps of product realization, from the idea to the marketable product: R&D, engineering, industrialization, quality, regulatory.
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Global Engineering, Quality & Regulatory Consulting Serving Manufacturers of Medical Device, Pharmaceutical and Biologics for Over 25 Years
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DMD Consulting - Medical devices
DMD Consulting - Medical devices
Parkdale Group Japan Medical Device Regulatory and Marketing
Japan Medical Device Market Entry PMDA management and consulting company. Japan Healthcare Technology and Medical Device strategy and consulting.
Rihim Pharma Consultancy (India) - Regulatory Consultants
Leading Regulatory Services for Pharma, Cosmetics & Medical Devices • DCGI (CDSCO) Services – Rihim Pharma Consultancy Pvt. Ltd.
Innolitics - Medical Device Software Services
We help medical device startups go from idea to acquisition with our regulatory and software-engineering services.
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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.
ChemSafe Consulting | Regulatory Affairs Experts
CHEMSAFE provides regulatory, technical, scientific and legal services for pharmaceutical, chemical, cosmetic, food and medical device companies
CMC MEDICAL DEVICES - YOUR QUALITYIS OUR SERVICE
EC REP of Medical Devices, Consultant of CE mark, ISO 13485, OBL Agreements, Regulatory Affairs
Medical Device Regulations Training | Semoegy Medtech Singapore
"MedTech companies will struggle less with medical device regulations if the regulatory requirements are seen as
Medicom Consulting, Irish medical devices consultants and consultants to the Medical industry
Medicom Consulting, Irish medical devices consultants and consultants to the Medical industry
AD Modum R&D | Research and development of medical devices
AD Modum R&D: research and development of medical devices with the max respect of the quality regulatory. Only the best services to healthcare companies.
MarcM Consulting Canada - Regulatory Affairs Consultants - Welcome
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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Nilo Medical Consulting Group
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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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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Whitney Consulting Ltd - China Medical Regulatory and Clinical Affairs
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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RCA Inc. | FDA and EU MDR Compliance & Regulatory Consultants
Regulatory Compliance Associates® Inc. (RCA) has global quality, regulatory & compliance expertise for medical device, pharmaceutical, biologics, combination products and compounding pharmacies.
Mexican Health Registry for Medical Devices
Regulatory affairs and technical consultancy services specialized in Mexican sanitary regulation of medical devices for obtaining health registry from COFEPRIS
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Medical Devices
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Consulting Services for Medical Device Companies
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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
Ours was Medical Device Contract Manufacturing & OEM Medical DeviceMedical Device Contract Manufacturing,OEM Medical Device
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The Tao of Excellence - Specialists for the medical devices industry
Specialists for the medical devices industry: services and solutions for regulatory strategy, quality management, certification, data analysis and training.
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Supports companies in Pharmaceutical, Medical Device and Cosmetics Industry. Regulatory Affairs, Quality Affairs, Pharmacovigilance Promotional Control
Accredited Consultants Pvt Ltd - Healthcare Regulatory Services
ACPL is one of the leading regulatory consultant service providers based in Delhi (India), for drugs, medical devices, food and cosmetics. We provide the complete range of services covering regulatory affairs, pharmacovigilance, clinical trial and medical writing.
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Medical Devices Quality Consulting Service and Medical Device Certification Consultant Service Provider | Operon Strategist, Pimpri Chinchwa
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MTC Medical Technology Consultants Germany
MTC is a consultancy offering regulatory and clinical services to the medical device industry world-wide
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Medical Device Consultants | Meddev Solutions UK
Meddev Solutions are an award winning team of Quality and Regulatory Consultants with over 65+ years of experience working in the medical device industry for both manufacturers and Notified Bodies. We provide solutions that work for your business first time, every time.
Medical Device Recruiters | Medical Device Recruiters
The medical device recruiters with the industry knowledge, personal approach, and proven process to bring your medical devices company the talent it needs.
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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Ivowen | Regulatory Affairs Specialists
Regulatory affairs consultancy specialising in human and veterinary pharmaceuticals, pharmacovigilance and medical devices
Medical Device & Pharmaceutical Consulting and Staffing Agency | Network Partners
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.
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Home | Medical and Regulatory Affairs Specialists
Preparing regulatory submissions for medical devices is a team marathon. Let us run a lap or two for you. You choose the pathway and set the milestones. We share the workload to help you finish strong. Robust, systematic literature reviews are key components of regulatory submissions. We run the ...
Author: Admin
Home - Medical Device Regulation and ISO quality standard
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Compass for Medical Device Development | Synergio
Compass guides medical device development teams through their product development and regulatory processes and make the creation of submission deliverables a fluid part of daily tasks.
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