1. WHO Expert Committee on Specifications for Pharmaceutical Preparations, Twenty-fifth Report, Technical Report Series 567, Geneva 1975. Deutsche Übersetzung: Revidierte GMP-Richtlinie (1978). Dtsch. Apoth. Ztg. 118:53
2. Department of Health and Social Security (1983): Guide to Good Pharmaceutical Manufacturing Practice. London, Her Majesty’s Stationery Office
3. Convention for the Mutual Recognition of Inspections in Respect of the Manufacture of Pharmaceutical Products (1985): Guidelines for Good Pharmaceutical Control-Laboratory Practice. Document PH 5/85, EFTA Secretariat Geneva
4. Department of Health, Education and Welfare, Food and Drug Administration: Good Laboratory Practice Regulations, Nonclinical Laboratory Studies. Federal Register Vol. 43, No. 247, December 22, 1978 p. 59986 to 60025 (USA)
5. Gesetz zum Schutz vor gefährlichen Stoffen (Chemikaliengesetz — ChemG) Bundesgesetzblatt 1980 Teil 1 S. 1718–1728