Non-commercial vs . commercial clinical trials: a retrospective study of the applications submitted to a research ethics committee

Author:

Fuentes Camps Inmaculada12ORCID,Rodríguez Alexis12,Agustí Antonia13

Affiliation:

1. Clinical Pharmacology Service; Hospital Universitari Vall d'Hebron; Barcelona Spain

2. Vall d'Hebron Research Institute (VHIR); Barcelona Spain

3. Department of Pharmacology, Therapeutics and Toxicology; Universitat Autònoma de Barcelona; Cerdanyola del Vallès, Barcelona Spain

Publisher

Wiley

Subject

Pharmacology (medical),Pharmacology

Reference19 articles.

1. Fact or fiction: the need for independent pharmaceutical policy research;Keyhani;J Gen Intern Med,2009

2. The continued need for independent research on prescription drugs;Hoadley;Health Aff,2004

3. Independent clinical research in Europe;Remuzzi;Lancet,2004

4. Impact assessment of the European Clinical Trials Directive: a longitudinal, prospective, observational study analyzing patterns and trends in clinical drug trial applications submitted since 2001 to regulatory agencies in six EU countries;Hartmann;Trials,2012

5. Directive 2001/20/EC of the European Parliament and the Council of 4 Apr 2001 on the approximation of laws, regulations and administrative provisions of the Member States relating to the implementation of good clinical practice in the conduct of clinical trials on medicinal products for human use;Anon;Official J Eur Community,2001

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