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Medidee Services - RA, CA/CRO and QA, for MedTech
Medidee: consulting in regulatory affairs, quality insurance, clinical affairs and digital health for medical devices and in vitro diagnostics.
CMC MEDICAL DEVICES - YOUR QUALITYIS OUR SERVICE
EC REP of Medical Devices, Consultant of CE mark, ISO 13485, OBL Agreements, Regulatory Affairs
Medical Device Consult - Medical Device Consult
Medical Device Consult is specialised in Medical Device and In-Vitro Diagnostic companies in meeting US & European regulatory...
confinis - regulatory compliance worldwide
confinis is a global consulting firm in the field of medical devices, in vitro diagnostics and combination products based in Switzerland and the USA. We are offering a wide range of services regarding combination products, product development, regulatory affairs, quality management, auditing & training.
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.
Author: GWK Präzisionstechnik GmbH
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.
Author: GWK Präzisionstechnik GmbH
Medical Device Consulting | QA/RA Consulting Group
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.
Medical Device Regulatory Consultants & QMS Specialists
Medical device regulatory consultants & quality management system specialists. Experienced partner passionate about the medical device industry.
Author: Motion Marketing
Acknowledge Regulatory Strategies
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
Medical Compliance Consultants | Sydney | ORA innovations
ORA Innovations: A leading provider of Medical Compliance Consulting Services for; Quality Management, Regulatory Affairs, Product Development, Product Licensing, and WH&S.
Medical Device Regulatory Consultants & More | Cofactortech.com
Cofactor Technologies provides international quality assurance and regulatory affairs consulting services to medical device companies worldwide.
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
Author: Motion Marketing
Medical Device + Diagnostic Industry
Medical Device and Diagnostic Industry (MD+DI)is the primary resource for manufacturers of medical devices and in vitro diagnostic products.
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Regulatory Affairs, Quality Affairs, Pharma Consultancy by Baggerman
Supports companies in Pharmaceutical, Medical Device and Cosmetics Industry. Regulatory Affairs, Quality Affairs, Pharmacovigilance Promotional Control
Florida Medical Device Consultant | FDA Regulatory Affairs Consultant
Medical Device Consultant Auditor 13485 FDA MDR CE Mark MDSAP Audit Florida Clinical Evaluation 510k 510(k) Internal Audit FDA Mock Audit FDA Mock Inspection PMA Regulatory Affairs Quality Management System MEDDEV 2.7/1 Rev 4 Orlando Tampa
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Medical Device Consultants offering ISO 13485 Quality Systems and Procedures and Medical Device Consulting Services
Acerna Inc. GMP Pharmaceutical Consultancy
Acerna is a pharmaceutical consultancy specialising in Good Manufacturing Practices, Quality Systems, and regulatory affairs including biological, medical device, and natural health products.
United Kingdom - PharmaLex
For companies in the global pharmaceutical, medical devices and healthcare industries that require expert advice and practical, hands-on support in regulatory affairs, pharmacovigilance and development consulting.
Author: PharmaLex @PharmaLexGLOBAL
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Trivitron Healthcare | medical devices companies
Trivitron Healthcare, a leading medical device company providing equipments and products to the healthcare industry. We offer a wide range of medical equipments & diagnostic products like medical Imaging Systems, Radiology Products, ICU & Operation Theater Products In-vitro Diagnostic Solutions and Newborn Screening Kits
Medical Equipment suppliers
V.M.Meditech, a leading medical device company providing types of equipment and products to the healthcare industry. We offer a wide range of medical equipments & diagnostic products like medical Imaging Systems, Radiology Products, ICU & Operation Theater Products In-vitro Diagnostic Solutions and Newborn Screening Kits
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
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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Regulatory Affairs Consultants Ireland, Pharmaceutical Regulatory Compliance Service
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An engineering and consulting partner for your design, quality management, CE-marketing and regulatory affairs for medical devices. Dr. Andreas Spiegelberg
Pro4People - Excellent IT Solutions for MedTech and IVD - Pro4People
Pro4People is a software house specializing in the development and delivery of innovative IT products for the global MedTech / IVD markets. We develop medical devices (MD), in vitro diagnostics (IVD) medical devices, the Internet of Medical Things (IoMT), cloud services, web and mobile applications. We offer IT infrastructure management and the delivery of launched cloud-based solutions, as well as quality, regulatory, and security consulting required to put a product on the market.
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ISS AG, Integrated Scientific Services, provides services to medtech companies for the development of medical devices and their introduction into the market. Typical services include embedded software development, regulatory and clinical affairs, quality management, qualification, and validation. The combination of scientific work methods with project management and software development capabilities gives ISS AG a unique position as a service provider for the medtech industry.
TS Quality & Engineering - Medical Device Consulting - TS Q&E - MDR
TS Quality & Engineering offers Medical Device Consulting Services for MDR, DHF, Risk Management, Product Development, UDI, EUDAMED, ISO 13485 certifications
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WQRE : WQRE - Wenmekers Quality & regulatory Expertise
Wenmekers Quality & regulatory Expertise. WQRE will provided support to medical device companies to comply with the world wide legislation on Quality and Regulatory related aspects. Our services cover all steps of a medical device development, from the initial project idea over the design & development to certification and/or regulatory clearance.
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Consulting im Bereich Med Tech Compliance für Quality Management und Regulatory Affairs ISO 13485, MDD, MDR, MDSAP, GMP 820
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Quality management consulting services tailored to your specific needs.Pharmaceutical Quality Assurance, Product Development, Regulatory Affairs.
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Homepage - Penman Consulting
Penman Consulting is a specialist consultancy providing a range of regulatory, technical and scientific services to companies in the chemical, petrochemical and fine chemical industries. Penman Consulting manages large industry REACH Consortia and has developed innovative product stewardship and regulatory affairs solutions for effectively managing chemical related information.
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PharmaLogika Quality Consultants specializes in Quality System and cGMP for the medical device, biopharmaceutical and pharmaceutical industries for FDA and Regulatory compliance.
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.
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.
Author: MarcM Consulting Canada
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Home - Northridge
Northridge Quality & Validation Validation and Quality Management for the Pharmaceutical and Medical Device Industries Northridge Quality & Validation provides services to the Medical Devices and Pharmaceutical Industries in the areas of Risk Management, Validation and Quality Systems. Our mission is to save Life Sciences companies time and money by carrying out projects in a […]
QSE - Quality Systems Engineering, Inc.
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.
AggreDyne | Diagnostic Device, Platelet Function Monitoring | Houston, TX
AggreDyne is a rapidly growing medical diagnostic company, whose focus is to develop best-in-class medical diagnostic tools that enable physicians and improve the patient experience. We are a “growth stage” company with FDA-cleared and CE marked in-vitro diagnostic products.
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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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your Consultant for Regulatory Affairs, GMP, GDP, GCP, GLP, Product Development, Quality Management, Übernahme der Fachtechnischen Leitung
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Regulatory and Quality consultancy company offering cervices for phamraceuticals, medical device, combination products, cosmetics and food supplements.
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Product development and project management support for medical device start-up companies.
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Learn about the first and only holistic Regulatory Information Management (RIM) software for medical device companies that consolidates all the functions of regulatory affairs.
Malaysia ISO Consultancy Company | Central Advisory System Official Website
Offering ISO Consultancy in Malaysia, Singapore; specialize is ISO 22000 haccp food safety management system, IRCA 13485 medical device management system
MFD & Associates - Home
"Providing Validation & Quality Systems Consulting to thePharmaceutical, Biotech, and Medical Device Industries"
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Lumin Logic is a premiere Medical Device Quality Management System used for medical device research, testing and regulatory compliance.
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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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Medical device consulting | Elseemed.ch | Ecublens VD
Elseemed.ch - Medical device consulting company, offering services for product development, software design, design control, risk management, project managment, and business analysis.
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ArtPharm Ltd.
ArtPharm Ltd. – quality management, pharmacovigilance, regulatory and safety management of pharmaceutical products and medical devices..
Medical Device QA/RA Consulting Services
Visit our website to connect with our experts to get medical device risk management consulting services that are 14971:2019 and ISO 13485:2016 compliant. Medical device risk management systems consulting services in the USA.
Author: MDR Consultants
Regulatory Affairs Compliance Consultants
Expert Regulatory Affairs consultants specializing in **** development, CMC regulatory, technical & project management for pharmaceutical, healthcare GMP, GCP
Author: Meranda Parascandola
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Directory of Medical Device Industry Suppliers Companies, Vendors, Products, and Services
Find device testing systems, medical tests, medical equipment, diagnostics devices, medical device research, testing devices and design, analytical and monitoring devices, surgical devices and medical device testing products. Compare companies providing device testing systems, medical tests, medical equipment, diagnostics devices, medical device research, testing devices and design, analytical and monitoring devices, surgical devices and medical device testing.
Medical Translation Services & Regulatory Affairs for Life Sciences
We are ISO13485:2016 & ISO9001:2015 certified to provide the highest quality medical translation services and regulatory affairs (RA) consulting services in over 150 languages and 60 countries, for pharmaceuticals, medical devices, CROs and other life sciences companies. Contact us for a consultative discussion today.
GxPconsult: The GCP Specialists
GcPconsult is specialised in quality assurance and regulatory compliance audits as well as related management consulting services.Our clients are from pharmaceutical, biotech, medical device industry.
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MWA is a consulting expert in quality systems and GXP compliance. We provide GAP Assessments, Mock GXP Regulatory Inspections for the pharmaceutical, biotechnology, cosmetics, dietary supplements & medical device industries.
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.
CE plus
CE plus is an international regulatory service provider for medical devices and in-vitro diagnostics, based in Badenweiler, in the immediate vicinity of Freiburg/Germany and Basel/Swiss. CE plus was founded in 2009 starting with profound operational experience in medical device and IVD industry as well as Notified Body business. With our dynamic “hands-on-mentality”, the service of CE plus extends far beyond traditional consulting.
Welcome | Masy Group GmbH
100+ audits and 10+ years experience within Quality (Assurance, System and Operations) in the Life Science Industry: Pharma, Medical Devices, In Vitro Devices and Biotech pharma, building up and improving robust GMP Quality Management System in Switzerland and Europe.
MEDICAL DEVICE DESIGN DEVELOPMENT | Helping develop products
Experts in medical device new product development and Quality Management support. Developing innovative technology for the healthcare industry.
Home - Strategic Regulatory Solutions
Strategic Regulatory Solutions is a company that offers Regulatory Affairs consultancy to the pharmaceutical industry. We specialise in the OTC industry and solutions to extend the product lifecycle.
Author: Michelle Riddalls
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Muller juridische diensten
Juridisch advies en begeleiding van personen en bedrijven bij juridische vragen, problemen en geschillen.
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