Companies Related to "Dorian Regulatory Affairs" [Most Relevant Company Matches] RSS

23:15 EST 14th December 2018 | BioPortfolio

Here are the most relevant search results for "Dorian Regulatory Affairs" found in our extensive corporate database of over 50,000 company records.

Showing "Dorian Regulatory Affairs" Companies 1–25 of 1,200+

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Dorian Regulatory Affairs

The company is located in the Netherlands and was founded early 1999 by Dorine Mulder, who had at that time 16 years experience in regulatory affairs in the pharmaceutical industry, including more than 8 years as Director Regulatory Affairs at the European headquarters of a major biotechnology company. Ms. Mulder has a doktoraal degree (Dutch M.Sc.) in biochemistry and an English M.Sc. degree in t...



TOPRA is the global organisation for Regulatory Affairs professionals and for those who have an interest in Regulatory Affairs in the healthcare sector.Our current membership is drawn from over 40 countries and members worldwide are actively involved in delivering the services needed by busy regulatory specialists. members are drawn from industry, the regulatory agencies and the consultancy commu...

DDN Medical Affairs

DDN Medical Affairs -- a member of the Dohmen family of companies -- offers medical and regulatory affairs support services for pharmaceutical, biotech and medical device companies. Established as a wholly-owned subsidiary of DDN, (which is a subsidiary of the 151-year-old Dohmen Company), DDN Medical Affairs is headquartered in Menomonee Falls, Wis...


Our mission as a team is to cooperate actively in research and marketing projects and regulatory affairs. Sharing our experience in the sector with laboratories/CROs.Recerca Clínica is a Spanish CRO founded in 2000, integrated by a group of professionals with more than 20 years experience in the sector.We adapt to each project needs, always offering quality service.We assess and support the execu...

Applied Logic Associates

Applied Logic Associates, Inc. (ALA) is a consulting firm for pharmaceutical, medical device and biotechnology companies in the areas of Clinical/Regulatory Affairs, Clinical Study Management, Information Management, Biostatistical Analysis and Health Care Economics. For 10 years, ALA has served as a vital link in bringing new products to market. ALA provides cost-effective and timely services fro...


AccuReg was founded in 1987 to serve the healthcare industries with expert regulatory, compliance and technical support. Our Associates are Regulatory Affairs professionals, chemists, engineers, biologists, quality specialists and technical writers with industrial and regulatory experience.

TopPharm Consulting

Regulatory affairs services in Poland. We are former Polish Authority experts who assessed dossier in national procedure, MRP, DCP, central procedure (EMEA) and were involved in preparation of Polish pharmaceutical regulations. Therefore besides common regulatory affairs services for medicinal products, medical devices and food supplements we can help you with scientific dossier preparation, liai...

Cyton Biosciences Ltd

Cyton Biosciences Ltd is a leading European consultancy company providing specialist product development and registration services to the global bioscience industries seeking product authorisations in Europe. Our eleven specialist scientists have more than 140 years cumulative experience of working within the bioscience industries and Cyton prides itself in harnessing this depth of experience to p...

M2 Worldwide

Clinical Services Clinical Trial Management System Biostatistics Data Management Regulatory Affairs Quality Assurance Non-Invasive Monitoring Document Control Medical Affairs Medical Writing

Med Exec International

To recruit and place top performing professionals in the fields of Clinical Research, Regulatory Affairs, Quality Assurance, and Medical Affairs quickly and effectively, with a focus on meeting the unique requirements of each assignment, enhancing value to industry projects, improving research processes and strengthening workplace capabilities

DSA Consultants

DSA Consultants is a full service consulting firm offering strategic guidance in Regulatory Affairs and Quality Compliance. We work with a wide range of companies to handle regulatory filings for drugs, biologicals, medical devices and other types of products. DSA Consultants has been in business for more than 20 years and has an established reputation in Canadian Regulatory Affairs. We handl...

Jacobsen Pharma A/S

Regulatory affairs specialists in Scandinavia and EU. We offer support on applications for marketing authorisation (national, MRP, DCP), readability testing of Patient Information Leaflets, pharmacovigilance, eCTD, variation and renewal applications, medical translations, can act as QPPV and more. For more information visit us at JACOBSEN PHARMA IS A DANISH COMPANY FOUNDED I...

Regulatory Affairs Professionals Society (RAPS)

The Regulatory Affairs Professionals Society (RAPS) is the leading worldwide member organization devoted to the health product regulatory profession. With more than 10,000 individual members from industry, government, research, clinical and academic organizations in more than 50 countries, RAPS develops professional standards for knowledge, competency and ethics and is the leading source of inform...

Medical Device Consulting

A Medical Device Industry Professional with experience to see the broad picture and the skills to developspecific solutions to complex problems in regulatory affairs, quality assurance, and manufacturing An ASQ Certified Quality Engineer active in the local section affairs A programmer of documentation and manufacturing control systems for medical device companies

The Medical Affairs Company LLC

The Medical Affairs Company LLC is a full service Contract Medical Organization that provides pharmaceutical, biotechnology, and medical device industry clients a wide array of outsourcing capabilities for medical affairs activities. Providing both strategic and tactical medical liaison support services in addition to medical liaison consulting and medical communications support, The Medical A...

Origin Pharmaceutical Services Limited

specializes in European clinical trials and regulatory affairs

CanReg Inc.

Anne Tomalin founded canreg in 1996 after working in regulatory affairs for more than 20 years at Wyeth, Roche and Searle. Her vision of a company dedicated specifically to regulatory affairs consulting addressed a large unmet need, especially for smaller companies. Today, canreg works with companies of all sizes and at all stages of development. Our most senior consultants have more than 30 ye...

Computer Chemistry Consultancy

Consultancy in the area of web-enabling of technical and scientific software, and in XML-services for Regulatory Affairs, R&D, IT, and Clinical Trials departments of pharmaceutical companies.

Pharmaceutical Strategic Initiatives, LLC

Pharmaceutical Strategic Initiatives, LLC (PSI) is the premier provider of strategic clinical and regulatory consulting, priority comparative effectiveness and outcomes research, scientific content creation, opinion leader development and management to Academic Institutions, Pharmaceutical, Medical Device and Biotechnology companies. For 26 years, PSI has supported Educational Programs and Worksho...

YRCR Limited

independent contract organisation providing regulatory affairs and development services to the pharmaceutical and healthcare industries.

Legacy MedSearch

Legacy MedSearch is a retained recruitment firm focused exclusively on the medical device and technology industry. The firm serves emerging, mid-sized and Fortune 500 medical device companies who require a specialized approach to placing C-level executives and senior managers in the areas of engineering, sales and marketing, research and development, produ...

Pharmaffair Incorporated

consulting firm for pharmaceutical, medical device and biotechnology companies in the areas of regulatory affairs and manufacturing.

AAM Biosimilars Council

The Biosimilars Council, a division of the Association for Accessible Medicines (AAM), works to ensure a positive environment for patient access to biosimilar medicines. The Biosimilars Council is a leading source for information about the safety and efficacy of more affordable alternatives to costly brand biologic medicines. Areas of focus include public ...


Our interdisciplinary teams take a prospective view of our clients' needs. We work closely with clients' marketing, business development, research and development, scientific and regulatory affairs, government affairs, and legal divisions, throughout all stages of a product's lifecycle.We enable our clients to:Evaluate the approval and over-the-counter switch potential of pharmaceutical and consum...


ArisGlobal ( is a leading provider of integrated software solutions for pharmacovigilance and safety, regulatory affairs, clinical research and medical information. Hundreds of life science companies rely on ArisGlobal’s advanced solutions for maintaining regulatory compliance, workflow automation, improving operational efficiency a...

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