Top 100 alternative sites to cmcmedicaldevices.es
Medical Device Consult - Medical Device Consult
Medical Device Consult is specialised in Medical Device and In-Vitro Diagnostic companies in meeting US & European regulatory...
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 Regulatory Consultants & More | Cofactortech.com
Cofactor Technologies provides international quality assurance and regulatory affairs consulting services to medical device companies worldwide.
ISO 13485 Quality Systems | Medical Device Consultants
Medical Device Consultants offering ISO 13485 Quality Systems and Procedures and Medical Device Consulting Services
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
Accelagen | Biopharmaceutical and Medical Device Development
Pharmaceutical and Medical Device Regulatory Affairs and Clinical Research Development Organisation
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
Regulatory Affairs Consultants Ireland, Pharmaceutical Regulatory Compliance Service
EMRC, Regulatory Affairs, Pharmaceutical, Consultancy, Advice, Medical Device, Registration, CE Marking , Wholesale Services
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.
Welkom bij QAid
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.
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
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
Expert Medical Device Consulting | US and EU | Kapstone Medical - Kapstone Medical
Kapstone Medical integrates with medical device companies at every stage of the product life cycle. Quality Assurance, Regulatory Affairs, Product Development and Manufacturing Solutions.
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
Medical Devices QMS and Regulatory Affairs Melbourne
We specialise in Quality Assurance and Regulatory Affairs for Medical Device companies, achieving 100% compliance for all our clients
Pharmaceutical and Regulatory consulting | Medical Devices
PDS is a pharmaceutical and regulatory consultancy serving the pharmaceutical, biopharmaceutical, medical device and cosmetic industries.
Author: Anicca Solutions A W-Fowler
Medicora GmbH - Pharma Consulting and Medical Services - Medicora GmbH - Pharma Consulting and Medical Services
Senior expert consultancy in market access, medical and regulatory affairs
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.
Author: Tradeline Medical Lab; USA
Other sites like cmcmedicaldevices es
Medical device regulatory, clinical, and technical services
Paladin Medical®, Inc. offers a full range of medical device regulatory, clinical, and technical services for premarket applications and regulatory compliance.
FDA Consultants | Medical device consultants | pharmaceutical consultants |
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 %
www.medtechcomp.ch - Quality Management ISO13485, Regulatory Affairs, Consulting Medical Device Compliance, Technical File STED Format, Mer
Consulting im Bereich Med Tech Compliance für Quality Management und Regulatory Affairs ISO 13485, MDD, MDR, MDSAP, GMP 820
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.
Medical Device Regulatory Consultants for EU MDR Compliance
Our team of Medical Device Regulatory Consultants are specialists offering tailored EU MDR Compliance services.
ARQon Singapore - Medical Device Consulting, Regulatory, Medtech
ARQon is a medical device consultant for Regulatory, Quality RA/QA, device registration, clinical trials, ISO13485, GDPMD, MDSAP and distribution consulting.
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.
Rømer Consulting – Regulatory Navigation for Medical Devices
Regulatory Navigation for Medical Devices
Innolitics - Medical Device Software Services
We help medical device startups go from idea to acquisition with our regulatory and software-engineering services.
Author: Innolitics; LLC
Consulting Services for Medical Device Companies
Consulting Services for Medical Device Companies
Author: RAYMED Medical Device Solutions
CE mark medical devices by Winckels Medical Devices Expertise WMDE
Click here for infromation about CE mark medical devices from WMDE
CE Certification - Medical Device CE Marking
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.
Home - Medical Device Regulation and ISO quality standard
Want to Master Medical Device Regulation & learn how to put a product on the market in Europe. Easy Medical Device is a platform for tools and resources for Regulatory Affairs, Quality Management, Regualtory Compliance. Learn how to choose your notified body or how the device regulation is different in other countries
Author: Monir El Azzouzi
Medical Devices Quality Consulting Service and Medical Device Certification Consultant Service Provider | Operon Strategist, Pimpri Chinchwa
Operon Strategist - Medical Devices Quality Consulting Service, Medical Device Certification Consultant & Medical Devices Compliance Service Service Provider from Pimpri Chinchwad, Maharashtra, India
Regulatory strategies & consultancy service for medical device manufacturers | MT Promedt Consulting
MT Promedt Consulting develops regulatory strategies and delivers innovative solutions to the needs of the medical device and **** industry. Find out more!
FPQ Consulting - Medical Device
Med 20 års erfarenhet av kvalitetsarbete med ISO standarder 9001 och 13485 har jag skapat en gedigen kunskapsbank, allt från produkt- och process specifika riskanalyser till en komplett CE-märkning av medicintekniska produkter. Kompetensområdet inom medicinteknik täcker många områden vilka beskrivs mer under fliken Tjänster. CE-märkning, Medical Device, 93/42, kvalitetsstyrning, interna revisioner, riskanalys, ISO 14971, ISO 13485, kvalitetsmanual, leverantörsbedömning, kvalitetschef, CAPA system, kvalitetschef, Medical Device Consultant, Frank Palm
Moody Consulting Pakistan - Medical Devices Compliances & ISO Certifications
Moody Consulting Pakistan deals in Medical Device Regulatory, GDPMD Implementation & Compliances, ISO Certifications & Auditing and Quality Assurance
Medical Device Registration System - Regulatory Consulting|LICENSALE®
LICENSALE® is a global medical device registration system that lets you take full control of your regulatory affairs and gain approvals in 140 countries.
Ours was Medical Device Contract Manufacturing & OEM Medical DeviceMedical Device Contract Manufacturing,OEM Medical Device
Ours was Medical Device Contract Manufacturing & OEM Medical Device. You are looking for manufacturer.We are Medical Device Contract Manufacturing and We are OEM Medical Device.
International Medical Device Regulators Forum
The purpose of the IMDRF is to accelerate international medical device regulatory harmonization and convergence
What else cmcmedicaldevices.es alternative websites
Tegra Medical | Contract Manufacturing Complex Medical Devices
Tegra Medical is the company where medical devices come to life. Contract manufacturing of complete finished devices and complex components.Experts in combining technologies to manufacture complicated devices. ISO 13485 and FDA QSR compliant. Massachusetts, Mississippi, and Costa Rica.
FDA consultant | MDR Solutions Co., Ltd. | Thailand
FDA Consultant | Regulatory Affair | Medical Device | Medical Robotics | Seminar/Lecture | MDR Solutions
Ivowen | Regulatory Affairs Specialists
Regulatory affairs consultancy specialising in human and veterinary pharmaceuticals, pharmacovigilance and medical devices
Veraque consulting. 我们满足您的需求
Veraque consulting provides regulatory affairs solutions in Mexico for medical devices and IVDs.
raPHARM regulatory affairs consulting and education
raPHARM is a consultancy and education office specialising in pharmaceutical and medical devices regulatory affairs.
DMD Consulting - Medical devices
DMD Consulting - Medical devices
Regulatory Expert Medical Devices
Niels Ole Andersen is a Regulatory Expert finding a pathway bringing Medical Devices to market with a pragmatic approach
Medical devices
China Medical Device is online Medical Device database of China Medical Devices and China Medical Device Suppliers.
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
Author: Waqas Imam
Medical Device Quality Management System | LuminLogic Software
Lumin Logic is a premiere Medical Device Quality Management System used for medical device research, testing and regulatory compliance.
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.
Quality Consultants ISO 9001 And ISO 13485 MDSAP
Quality programs and medical device regulatory consulting, ISO 13485:2016 MDSAP program, employee training and internal audits, Toronto
Medical Device Reprocessing Consulting Services in ON
Medical Device Reprocessing Consulting Services offers consultation, training, and other services to help clients in ON comply with current best practices.
Medicom Consulting, Irish medical devices consultants and consultants to the Medical industry
Medicom Consulting, Irish medical devices consultants and consultants to the Medical industry
Medical Device Distributor | Australia | Device Matters
Device Matters is an independent consultancy and distributor of medical device technologies across Australia and New Zealand.
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
Author: Whitneyconsulting
Medical Device Regulations Training | Semoegy Medtech Singapore
"MedTech companies will struggle less with medical device regulations if the regulatory requirements are seen as
CRO Services | Avion Medical | Hawthorn
Avion Medical is your specialist health solutions partner from Research to Commercialisation – we provide consulting, medical affairs and clinical research services for pharma, biotech and medical devices
European Authorized Representative - Consulting CE Marking - CMC Medical Devices
European Authorized Representative and Consulting CE Marking. CMC Medicaal is an official European Authorized Representative and Consulting CE Marking.
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.
Other websites similar as cmcmedicaldevices.es
Jiangsu Bonss Medical Technology Co., Ltd. - Medical Devices (Medical Device, Surgical Device
Jiangsu Bonss Medical Technology Co., Ltd., Experts in Manufacturing and Exporting Medical Devices (Medical Device, Surgical Device and 355 more Products.
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.
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.
Medical Device Marketing | Device Lead Generation | Medical Marcom
Medical Marcom is a medical device marketing consultancy specializing in marketing communications, strategy, lead generation, web development, social media.
Infratech Medical Devices, Inc. | Medical Devices
Medical Devices
China SFDA Approval and Registration for Medical Devices, SFDA Registration Agent service
World-leading Wellkang Consulting group help you with China SFDA Approval and Registration for Medical Devices, SFDA registration agent service. One-stop information & guide on China's SFDA regulatory issues.
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.
Spiegelberg Consulting, Spiegelberg Zurich, Spiegelberg, Andreas Spiegelberg, Dr. Andreas Spiegelberg
An engineering and consulting partner for your design, quality management, CE-marketing and regulatory affairs for medical devices. Dr. Andreas Spiegelberg
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.
Susanne Merk | Regulatory Medical Writing | Medical Devices
Nutzen Sie das Plus an Expertise aus langjähriger Industrieerfahrung und konsequenter Weiterbildung. Regulatory Medical Writing umfasst Klinische Daten für die Marktzulassung und Erstattung, die Klinische Bewertung MEDDEV 2.7.1. sowie Medical Devices.
MTC Medical Technology Consultants Germany
MTC is a consultancy offering regulatory and clinical services to the medical device industry world-wide
Author: Gerd Juhl
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