Legal requirements for the preclinical toxicological evaluation of biomaterials
Tài liệu tham khảo
Bundesgesetzblatt, 1976
Produkthaftungsgesetz, 1990
1989, Bundesgesundheitsblatt, 32, 108
Commission of the European Communities, 1990, The active implantable medical device directive, Official Journal of the European Communities, L 189
Commission of the European Communities, 1990
US Department of Health and Human Services Public Health Service, 1985
US Department of Health and Human Services Public Health Service, 1986
US Department of Health and Human Services Public Health Service, 1987
US Department of Health and Human Services Public Health Service, 1987
Autian, 1973, Toxicogenic potentials of biomaterials and methods for evaluating toxicity, Med. Instrum., 7, 125
US Department of Health and Human Services, 1987
Autian, 1980, Plastics
Franck, 1987
Commission of the European Communities, 1983, Council Recommendation of 26 October 1983 Concerning Tests Relating to the Placing on the Market of Proprietary Medicinal Products (83/571/EEC), Official J. Europ. Commun., L 332, 11
World Health Organisation, 1969, Principles for the Testing and Evaluation of Drugs and Carcinogenicity, WHO Techn. Rep. Ser. 426
American Society for Testing and 'Materials (ASTM), Philadelphia, Pennsylvania, USA.
Biologische Prüfungen von Dentalwerkstofffen, DIN V 13930, Beuth Verlag GmbH, Berlin, 1987.