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Heads of Medicines Agencies: About HMA
Startseite - DGRA e.V. - Deutsche Gesellschaft für Regulatory Affairs
Die Deutsche Gesellschaft für Regulatory Affairs e.V. ist eine wissenschaftliche Fachgesellschaft im Bereich der Zulassung von Arzneimitteln und bietet den Studiengang Master of **** Regulatory Affairs an.
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Freyr is a Global Regulatory Solutions and Services company, focusing on the entire Regulatory value-chain ranging from Regulatory Strategy, Intelligence, Dossiers, Submissions to post approval maintenance, Labeling, Artwork Change Management for Pharmaceutical, Generics, Medical Device, biotechnology, Biosimilar, Consumer Healthcare, Cosmetic companies across the globe.
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Join the leading English language school in Cardiff (UK). Online and in-person courses accredited by the British Council and IALC.
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Nonclinical Consulting (Pharmacology, Pharmacokinetics, Toxicology) -
Nonclinical Project Development - **** Regulatory
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Regulatorium
Welcome
RegLek Regulatory affairs — RegLek Regulatory affairs
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Vet CRO Löhlein and wolf GbR vet research and consulting is a veterinary contract research organisation providing services in project management, monitoring, medical writing and quality assurance - for veterinary clinical studies in animal health.
Durapharm
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LINDH Teknik hjälper dig med CE Märkning mot EMC direktivet 2014/30/EU, LVD direktivet 2014/35/EU, MD direktivet 2006/42/EC och CE direktivet. Vi utför: avstörning, provningar, certifiering, PCB design, rådgivning, och elsäkerhet konsultationer mm.
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VeirupConsult - Regulatory Affairs siden 1995
Regulatory Affairs, Pharmacovigilance, GDP, danish/english version
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MARAS AG – Regulatory Affairs
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The Rosewood Group
The Rosewood Group is nationally recognized as one of the top executive search firms in the United States.
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VIGILIT - Pharmacovigilance Literature Management and Retrieval System
Pharmacovigilance Literature Management and Retrieval System -Literaturdatenbank mit arzneimittelsicherheitsrelevanten Ver?ffentlichungen sowie die Bestellung von Artikeln und CIOMS Meldeb�gen
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regenold GmbH
regenold GmbH is specialised in development, international regulatory affairs and market access. Founded in 1994, we have helped many clients gain marketing authorisations for their product developments both nationally and internationally.
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Zenosis is a web-based library for eLearning Pharmaceutical in the EU & USA. We have an extensive knowledge base to teach Pharmaceutical & Biotechnology Compliance.
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Canadian Association of Professionals in Regulatory Affairs | CAPRA
BEQS
Bacchus Engineering & Quality Solutions for Medical Manufacturing Consulting
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Ralf Jauster Produktentwicklung und Medizintechnik seit 1991 Product Development and Medical Devices
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Die JKorus GmbH in Zug bietet Ihnen Unterstützung bei der Planung und Umsetzung der neuen Anforderungen der MDR & IVDR und sämtlichen Themen rundum Entwicklung, Compliance, weltweite Zulassung und Qualitätsmanagement an.
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Roger Dallwig Clinical Research Services
Thorburn Geiger Group
Thorburn Geiger Group - International Management Consultants
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Pharma Search Partners, Inc. is a pharmaceutical industry placement service specializing in the placement of highly skilled professionals in
Pharma Search Partners, Inc. is a pharmaceutical industry placement service specializing in the placement of highly skilled professionals in permanent or temporary positions in such fields as Pharmacoeconomics, Pharmacoepidemiology, Medical Directors Regulatory, Compliance and Manufacturing. We have set up teams in the UK, India, and Singapore, to name a few. Our recruiters have pharmaceutical industry experience ranging from pre-clinical research, clinical research, sales & Marketing, regulatory affairs, quality assurance, and information technology, research and development and Medical Affairs.
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DSA Consultants are your partner for regulatory affairs and GMP quality compliance in Canada: drugs, pharmaceutical, natural health products, and cosmetics.
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www.rautakisolutions.com. Rautaki Solutions is an international consultancy business specialising in supporting innovation and excellence. Our services support Business Development, Regulatory Affairs and Risk Management, Strategic and Risk Comms.
News, opinion, and analysis for the Pharmaceutical and **** Manufacturing Industry - EPM Magazine
European Pharmaceutical Manufacturer magazine: Breaking pharmaceutical and pharma manufacturing news, opinion and analysis - Including the latest breakthroughs in pharma, **** delivery, formulation, R&D, packaging, finance & investment, logistics & distribution, manufacturing, and pharma supply chain
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NIPCOS CONSULTING
your Consultant for Regulatory Affairs, GMP, GDP, GCP, GLP, Product Development, Quality Management, Übernahme der Fachtechnischen Leitung
Prof. Dr. Marco Althaus
Website von Prof. Dr. Marco Althaus, Politikwissenschaftler, Technische Hochschule Wildau
FAQ Consulting - Innovations & Impact
Author: Ulrich Schwanke
Dr. Matthias Brunner – Entrance
Dr. Matthias Brunner, **** Regulatory Affairs Consultant
Author: Dr Matthias Brunner
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Revipharm is a consulting firm which provides a wide range of consultancy services to the pharmaceutical industry from initial regulatory strategy, to the Marketing Authorisation approval, marketing and ongoing lifecycle management.
Regulatory affairs Rejestracja leków
SCPC - Salt City Pharma Center zajmuje się rejestracją produktów leczniczych -leków, rejestracją wyrobów medycznych, rejestracją suplementów diety, rejestracją kosmetyków, tłumaczeniami medycznymi oraz pharmacovigilance
MC TOXICON
MC Toxicology Consulting supports **** development by designing tailored, product- and indication-specific non-clinical programs.
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Tiare Consulting | Consultora de registros
Tiare Consulting, consultora de gestiones regulatorias que afecten a la industria alimentaria, farmacéutica, veterinaria y parafarmacéutica.
KCR | Full-service CRO | Clinical Development
KCR is an international full-service contract research organization providing clinical development solutions for the biotechnology and pharmaceutical industries.
Author: Mike Jagielski; KCR CEO
Regulatory Affairs Consultants Ireland, Pharmaceutical Regulatory Compliance Service
EMRC, Regulatory Affairs, Pharmaceutical, Consultancy, Advice, Medical Device, Registration, CE Marking , Wholesale Services
Die politische Verantwortung deutscher Unternehmen
Bundes- und Landtagswahlen werden von politischen Faktoren bestimmt, die die politischen Rahmenbedingungen stark verändern: liquide Demokratie, Bürgerbewegungen, informationelle Rasanz.
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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.
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The American College of Clinical Pharmacology (ACCP) is a 501 (c)(3) non-profit organization that is dedicated to advancing clinical pharmacology to enhance patient care.
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