1. Guidelines for preclinical toxicity testing of investigational drugs for human use;FDA (Food and Drug Administration),1968
2. Directives: 75/318/EEC and 75/319/EEC: Commission recommendation to the Member States concerning tests relating to the placing on the market of proprietary medicinal products;EEC (European Economic Community);Official Journal EEC,1975
3. Guidelines for the assessment of drug and medical device in animals;PMA (Pharmaceutical Manufacturers Association),1977
4. Appraisal of the safety of chemicals in foods, drugs and cosmetics;FDA (Food and Drug Administration),1959
5. Directive 83/570/EEC: Modification to Council directives 65/65, 75/318 and 75/319. (For marketing authorization for proprietary medicinal products in the Member States of the European Community on the use of the new multi-state procedure.);EEC (European Economic Community);Official Journal EEC,1983