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Medical Device Consultants – Regulatory Affairs Specialist
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.
Author: Adminqara
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
Medical Device Regulatory Consultancy | EU Medical Device Regulation
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
Medizinprodukte QM und Regulatory Affairs Beratung
Beratung für Hersteller von Medizinprodukten - Qualitätsmanagement (QM) nach ISO 13485 und CE-Zertifizierung von Medizinprodukten und In-vitro-Diagnostika.
Medical Device Regulatory Consultants & More | Cofactortech.com
Cofactor Technologies provides international quality assurance and regulatory affairs consulting services to medical device companies worldwide.
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
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.
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
Rømer Consulting – Regulatory Navigation for Medical Devices
Regulatory Navigation for Medical Devices
Medical Device Regulatory Consultants for EU MDR Compliance
Our team of Medical Device Regulatory Consultants are specialists offering tailored EU MDR Compliance services.
KD&A – Regulatory consultants for Medical and IVD Devices
Author: KD; A
AtlantiQ Consulting | Medical Devices | Quality | Regulatory
Freelance consultant with +25 years of experience in medical devices, including sterile and / or implantable 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 Device Regulatory Experts
Experts in FDA and EU medical device regulation and Food Safety (FSMA) regulations
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.
P.SS.T – Consulting in Regulatory Affairs
Regulatory Affairs Compliance Consultants
Expert Regulatory Affairs consultants specializing in **** development, CMC regulatory, technical & project management for pharmaceutical, healthcare GMP, GCP
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Regulatory affairs regulatory consulting services Poland
TopPharm: Pharmaceutical regulatory affairs and regulatory consulting services in Poland and EU. We are former authority experts.
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Medical Device Consult - Medical Device Consult
Medical Device Consult is specialised in Medical Device and In-Vitro Diagnostic companies in meeting US & European regulatory...
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
GENICOMMS - Medical Communications & Regulatory Affairs
We are a Medical Communications & Regulatory Affairs agency based in Switzerland.
Regulatory Affairs Consulting Firms & Services Australia | Regulatory Consultants
Gain control of your production process or require regulatory affairs consulting services in Austrlaia. Regulatory Matters helps you develop to standards.
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
Global Medical Device Consulting – Regulatory, Quality, Clinical | Emergo
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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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We pride ourselves in developing practical and sensible solutions to sometimes complex regulatory and legal issues.
FDA Regulatory Affairs Biotechnology Consultants
Engagiert im Pharma-Consulting und in Regulatory Affairs
Diapharm ist eine international führende Dienstleistungs- und Beratungsgesellschaft für die Pharma-, OTC- und Consumer-Healthcare-Industrie.
Diapharm | Regulatory Affairs und Pharma Consulting
Diapharm ist eine international führende Dienstleistungs- und Beratungsgesellschaft für die Pharma-, OTC- und Consumer-Healthcare-Industrie.
ChemSafe Consulting | Regulatory Affairs Experts
CHEMSAFE provides regulatory, technical, scientific and legal services for pharmaceutical, chemical, cosmetic, food and medical device companies
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raPHARM is a consultancy and education office specialising in pharmaceutical and medical devices regulatory affairs.
Regulatory Affairs Consulting - Gabriella Wechsler
Pharmadvice - An Independent Regulatory Affairs Consultancy
Since 2002 PharmAdvice has been working as an independent Danish consultancy company, specialised in the fields of Pharmacovigilance, Regulatory Affairs and Marketing Compliance and Support. We add core value to our customers using our experience, knowledge, dedication and commitment.
RegLek Regulatory affairs — RegLek Regulatory affairs
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Regulatory Affairs
Regulatory Affairs Consultants (RAC) Netherlands provides RA services to the pharmaceutical/biotech industry on European **** Regulatory Procedures. Our services range from the pre-marketing authorisation application (MAA) phase to the post-MAA phase, including the application for reimbursement (in...
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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!
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.
Andaman Medical: Regulatory Affairs & Market Access
Andaman Medical specializes in the registration, representation, importation & master distribution of medical devices & IVDs in Southeast Asia.
Regulatory Affairs Consultants Ireland, Pharmaceutical Regulatory Compliance Service
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pharmaceutical products, medicines, regulatory affairs, application procedures, Chemistry Manufacturing Control (CMC), Stability Testing, Quality by Design, Release (RTR), Process Analytical Technology (PAT), Quality Control, Good Manufacturing Practice (GMP), Quality Assurance, Inspection, Anti-counterfeiting, Qualified Person (QP), CTD Module 3, training, courses
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
Regulatory, Clinical Consulting Services to Biopharma & Medical Device Companies | MakroCare
Regulatory Affairs Jobs Ireland | Regulatory Affairs Careers
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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.
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CaRACS - Clinical and Regulatory Affairs Consulting Services
CaRACS - Clinical and Regulatory Affairs Consulting Services, is dedicated to Clinical Development Strategy and Regulatory Affairs Consulting Services for biotechnology and pharmaceutical industries.
Author: Michael Beckert
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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CaRACS - Clinical and Regulatory Affairs Consulting Services
CaRACS - Clinical and Regulatory Affairs Consulting Services, is dedicated to Clinical Development Strategy and Regulatory Affairs Consulting Services for biotechnology and pharmaceutical industries.
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CaRACS - Clinical and Regulatory Affairs Consulting Services
CaRACS - Clinical and Regulatory Affairs Consulting Services, is dedicated to Clinical Development Strategy and Regulatory Affairs Consulting Services for biotechnology and pharmaceutical industries.
Author: Michael Beckert
TPRAC - The Pharma Regulatory Affairs Consultancy in Chennai
CaRACS - Clinical and Regulatory Affairs Consulting Services
CaRACS - Clinical and Regulatory Affairs Consulting Services, is dedicated to Clinical Development Strategy and Regulatory Affairs Consulting Services for biotechnology and pharmaceutical industries.
Author: Michael Beckert
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CaRACS - Clinical and Regulatory Affairs Consulting Services
CaRACS - Clinical and Regulatory Affairs Consulting Services, is dedicated to Clinical Development Strategy and Regulatory Affairs Consulting Services for biotechnology and pharmaceutical industries.
Author: Michael Beckert
A-pharmaconsult - consultants in Regulatory affairs and Quality Assurance
Regulatory Affairs Consulting Company in Ontario, Canada
We are a full-service regulatory affairs consulting company providing consultation, license, and compliance for cannabis & natural health products in Canada.
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
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Integrated Regulatory Outsourcing from Regulatory Professionals, specialising in recruiting for pharmaceutical regulatory affairs vacancies.
Woodley BioReg Regulatory Affairs, Compliance and Conformance for pharmaceutical, biopharmaceutical, healthcare, API and Medical device manu
Woodley BioReg helps pharmaceutical, biopharmaceutical, healthcare, active pharmaceutical ingredient manufacturers companies develop & manufacture products
MARAS AG – Regulatory Affairs
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Die orangeglobal group ist Spezialist für Regulatory Affairs und Prozessoptimierung für Pharma und Medizinprodukte und strategischer Partner während der gesamten Internationalisierung.
Regulatory Affairs in VietNam
Vietnam Regulatory Affairs Society - VNRAS - Cộng đồng đăng ký thuốc tại Việt Nam
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Regulatory Affairs | PRSG
regulatory affairs, dossier creation, consulting, maintenaince
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.
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Dans l'oeil de son reflex (et de ses amis)
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