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Regulatory Affairs Consulting

Medical device regulatory affairs consultants ensure that companies follow the regulations set by FDA or other regulatory bodies around the world. They may assist with regulatory submissions, compliance, or postmarket surveillance of products, in addition to other activities. In this directory, you'll find knowledgeable regulatory affairs specialists focusing on the medical device industry.

Companies (15 results)

Featured
WEST Pharmaceutical Services Inc.

WEST Pharmaceutical Services Inc.

About Us West is a leading global manufacturer in the design and production of high-quality, techn...

Featured
BeanStock Ventures

BeanStock Ventures

BeanStock Ventures is 1 of 9 FDA-accredited Third Party Review Organizations globally. We provide software development a...

Regulatory Specialists, Inc

Regulatory Specialists Inc. is a team of skilled FDA and international medical regulatory consultants in th...

Avania

San Diego, CA USA. Qualifications: ISO 9001. Markets Supplied: Worldwide.

Biomed Research Inc.

Contact: Michael DaytonYear Established: 1997No. of Employees: 10Key Clients: Johnson & Johnson, Bausch & Lomb, Storz...

Biomedical Devices of Kansas LLC

Biomedical Devices of Kansas LLC (BMDK), qualified under FDA QSR (21CFR 820) was formed in 2006. Si...

Biopharmaceuticals Consulting Group

Contact: Fatieh Saless, PhD Year Established: 1999Biopharmaceuticals Consulting Group offers se...

Freyr Solutions

Freyr is a Global Regulatory Partner offering a full suite of regulatory services for global regulatory compliance requiremen...

NEO Tech (NEO Technology Solutions)

NEOTech combines the strengths of three leading contract manufacturers: NATEL, EPIC, and OnCore...

MDRS, LLC

MDRS, LLC, an FDA registered company, founded in 2010, provides regulatory, product development, quality and clinical research solutio...

Business & Decision Life Sciences

Contact: Keri Collette Business & Decision Life Sciences is part of an international Consulting an...

Donawa Lifescience Consulting Srl

DLC, headquartered in Rome, Italy, and founded by a former US FDA CDRH official who serves as Pres...

MEDevice Services LLC

MEDevice Services (MDS) provides personalized, cost-effective FDA and Health Canada regulatory- and quality-related ...

RJR Consulting

RJR Consulting, Inc. is a global life sciences regulatory compliance company founded in 2002, serving businesses, organization...

VISAMED GmbH

In order to shorten the product development cycle, medical device manufacturers need to identify as early as possible the world-w...

Products (3 results)

3P510K

3P510K

BeanStock Ventures

BeanStock Ventures is a FDA-Recognized 510(k) Third Party Review Organization which means we can review select 510(k) device submissions o...

Regulatory & Quality Consulting

Regulatory & Quality Consulting

BeanStock Ventures

We provide a range of software regulatory services including but not limited to: • Regulatory S...

Starter & DIY Software Regulatory Kits

Starter & DIY Software Regulatory Kits

BeanStock Ventures

Our DIY Regulatory Kit includes free and low cost resources: • On-demand - training ...

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