| Literature DB >> 11273440 |
Abstract
Good Clinical Practice is an international quality standard for conducting trials that involve participation of human subjects. Currently, the most widely accepted international document forming the base for GCP is the ICH Harmonised Tripartite Guideline for GCP, which defines in detail the responsibilities and obligations of parties engaged in clinical research. The purpose of this paper is to analyse how compliance with GCP provides protection of the trial subjects and assures quality and credibility of the data obtained.Entities:
Keywords: Biomedical and Behavioral Research; International Conference on Harmonization
Mesh:
Year: 2000 PMID: 11273440 DOI: 10.1007/s11948-000-0025-z
Source DB: PubMed Journal: Sci Eng Ethics ISSN: 1353-3452 Impact factor: 3.525