Browse a Listing
Top > Consulting > Medical and Life Sciences > Regulatory Affairs
Popular Tags
Web Links
An independent regulatory and scientific consultant who provides assistance to pharmaceutical, health product and chemical manufacturers for them to meet the requirements of government agencies.
Category:
Date Added: Aug 5, 2008 Hits: Rating: 0.00 Votes: 0
Member Reviews
Visitor Ratings
Google PR
German consultant for the pharmaceutical industry.
Category:
Date Added: Aug 5, 2008 Hits: Rating: 0.00 Votes: 0
Member Reviews
Visitor Ratings
Google PR
Consulting firms specializing in supporting hospitals, physicians and attorneys address complex coding issues. Major emphasis on working with counsel in support of fraud and abuse allegations from third-party payers.
Category:
Date Added: Aug 5, 2008 Hits: Rating: 0.00 Votes: 0
Member Reviews
Visitor Ratings
Google PR
, ideal for GxP compliance training requirements in the pharmaceutical or medical device industries.
Category:
Date Added: Aug 5, 2008 Hits: Rating: 0.00 Votes: 0
Member Reviews
Visitor Ratings
Google PR
German consulting group experienced in different licensing procedures of drugs and medicinal products at the national and European level. Website is available in both German and English.
Category:
Date Added: Aug 5, 2008 Hits: Rating: 0.00 Votes: 0
Member Reviews
Visitor Ratings
Google PR
Reg123.com is a portal for the new medicinal product development community with a focus on regulatory affairs and the pharmaceutical drug development process.
Category:
Date Added: Aug 5, 2008 Hits: Rating: 0.00 Votes: 0
Member Reviews
Visitor Ratings
Google PR
European pharmaceutical/biotech consultancy specializing in project management, medical writing, and business development.
Category:
Date Added: Aug 5, 2008 Hits: Rating: 0.00 Votes: 0
Member Reviews
Visitor Ratings
Google PR
European pharmaceutical GxP Consultancy.
Category:
Date Added: Aug 5, 2008 Hits: Rating: 0.00 Votes: 0
Member Reviews
Visitor Ratings
Google PR
Regulatory affairs consultancy headquartered in North Carolina.
Category:
Date Added: Aug 5, 2008 Hits: Rating: 0.00 Votes: 0
Member Reviews
Visitor Ratings
Google PR
A resource for issues surrounding the FDA's 21 CFR Part 11 Rule on electronic records and signatures.
Category:
Date Added: Aug 5, 2008 Hits: Rating: 0.00 Votes: 0
Member Reviews
Visitor Ratings
Google PR