healthcare / regulatory affairs

As a firm of health product experts, Shotwell and Carr, Inc., specializes in maximizing cost effectiveness in the development, approval, production and distribution of human and animal health products. Working within the ever-changing regulatory environment

biotechnology, biopharmaceutical, medical devices, FDA, regulatory affairs, HIPPA, 21CFR11, clinical research organizations, CRO, clinical trial, data management systems

ICON is a clinical research organisation (CRO) providing clinical research, drug development, regulatory affairs, laboratory services and imaging to the pharmaceutical and biotech industry

Assist manufacturers in bringing new medical technologies to the European market efficiently and cost-effectively

MeddiQuest Limited - Regulatory Affairs Management

The RegSource Regulatory page is a comprehensive site to information resources for the pharmaceutical professionals. The site provides links to regulatory and scientific information on the Internet for drug discovery, development and the drug approval process. Links are provided to full text information from the Federal Register (FR) and the information in the FR is focused by therapeuti...

Authorized Representatives for CE Mark, MDD, IVDD and European regulatory affairs, MDSS is an authorized european address, an authorized responsible person and authorized representative in the medical device industry

regulatory affairs professionals information, new medicinal product development guidelines, usa, uk

Smelt Werving & Selectie, Executive Search, Detachering binnen de farmaceutische & healthcare industrie. Altijd vacatures voor Artsenbezoekers, Product Specialisten, CRA's, Datamanagers ...

Regulatory Affairs, Connecticut, FDA, Medical Device, Quality, ISO, 510(k), Consulting

PAREXEL offers a range of services to assist the pharmaceutical, biotech, and medical device industries in bringing new products to market.

Panafarma Medical Consult AB

Kendle - What we do - Regulatory Affairs