Toxicity studies of biomedical products

Author:

Remya N.S.,Sangeetha V.P.,Mohanan P.V.

Publisher

Elsevier

Reference41 articles.

1. 10993-11 I. (2017). Biological evaluation of medical devices Tests for systemic toxicity. Vol 10993: ISO.

2. 11737-2 I. (2019). Sterilization of health care products-Microbiological methods. Tests of sterility performed in the definition, validation and maintenance of a sterilization process: ISO.

3. Non-clinical studies in the process of new drug development - Part II: Good laboratory practice, metabolism, pharmacokinetics, safety and dose translation to clinical studies;Andrade;Brazilian Journal of Medical and Biological Research=Revista Brasileira de Pesquisas Medicas e Biologicas/Sociedade Brasileira de Biofisica. [et al.],2016

4. Anon. (2010). Federal food, drug and cosmetics act. Silver Spring, MD, USA: US Food and Drug Administration. Available from: http://www.fda.gov/RegulatoryInformation/Legislation/FederalFoodDrugandCosmeticActFDCAct/default.htm

5. Improving prediction of carcinogenicity to reduce, refine, and replace the use of experimental animals;Bourcier;Journal of the American Association for Laboratory Animal Science,2015

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