Drugs, prescribed | Licensing and registration

Encyclopedia of Forensic and Legal Medicine

Volumn , Issue , 2005, Pages 239-242

  Sewell, G J ^a  

^a UNIVERSITY OF BATH   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 34548602932     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1016/B0-12-369399-3/00136-1     Document Type: Chapter

References (9)

1. S Bouayed The European Agency for Evaluation of Medicinal Products (EMEA) European Journal of Hospital Pharmacy 9 2003 38.
2. Commission of the European Communities The rules governing medicinal products in the EC, vol. 1 Pharmaceutical Legislation: Medicinal Products for Human Use 1998 Office for Official Publications of the EC Luxembourg.
3. Commission of the European Communities The rules governing medicinal products in the EC, vol. 3 Medicinal Products for Human Use: Guidelines 1998 Office for Official Publications of the EC Luxembourg.
4. Commission of the European Communities The rules governing medicinal products in the EC, vol. IV Good Manufacturing Practice for Medicinal Products 1998 Office for Official Publications of the EC Luxembourg.
5. Commission of the European Communities The rules governing medicinal products in the EC, vol. IX Pharmacovigilance 1998 Office for Official Publications of the EC Luxembourg.
6. Department of Health. The Medicines Act 1968 and its Various Orders and Statutory Instruments. London: HM Stationery Office.
7. Medicines Control Agency Rules and Guidance for Pharmaceutical Manufacturers and Distributors 2002 2002 Medicines Control Agency London.
8. MHRA Towards Safe Medicines. A Guide to the Control of Safety, Quality and Efficacy of Human Medicines in the United Kingdom 1997 MHRA London.
9. World Health Organization Requirements for the Collection, Processing and Quality Control of Blood, Blood Components and Plasma Derivatives. WHO technical report series no. 840 (annex 2), Geneva: WHO.