12. Composition and responsibilities of ethics committees and investigators

Acta Tropica

Volumn 78, Issue SUPPL. 1, 2001, Pages

  Ofori Anyinam, Opokua ^a  

^a GLAXOSMITHKLINE BIOLOGICALS   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 33644695109     PISSN: 0001706X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (5)

1. th General Assembly, Somerset West, Republic of South Africa, October 1996.
2. Council for International Organizations of Medical Sciences (CIOMS), in collaboration with the World Health Organization (WHO). International Ethical Guidelines for Biomedical Research Involving Human Subjects. Geneva 1993.
3. World Health Organization (WHO). Guidelines for Good Clinical Practice (GCP) for Trials on Pharmaceutical Products. World Health Organization Technical Report Series No 850 (1995); 97-137.
4. International Conference on Harmonization of Technical Requirements for the Registration of Pharmaceuticals for Human Use (ICH). Note for Guidance on Good Clinical Practice (CPMP/ICH/135/95) 1 May 1996.
5. Code of Federal Regulations, Title 21, Part 312, section 60 (US Government printing office, Washington DC. 1 April 1995.