ГОСТ Р ИСО 10993-11—2009
Библиография
1 Общая литература
(I) U.S./ЕРА РВ 86/108958 and 89/124077
12] U.S./FDA Toxicological principles for the safety assessment ofdirectfood additives. 1982
(3) U.S. Code of Federal Regulation 1500.40: Method ofTesting Toxic Substances
(4) United States Pharmacopoeia 26. Biological Reactivity Tests. In Vivo; The National Formulary 21. Rockville. MD;
Pharmacopoeial Convention. 2003, pp. 2028—2032
(5) ASTM F619-03. Standard Practice for Extraction of Medical Plastics
]6] SN 119800.1990. Biological Evaluation of Dental Materials
[7] European Pharmacopoeia 4th Edition. 2002
18] MHLW Notification No. 0213001(2003.02.13): Principles for Biological Safety Evaluation of Medical Devices
(9] HALLE. W. (2003) The Registry of Cytotoxicity: Toxicity testing in cell cultures to predict acute toxicity (LD^,) and to
reduce animal testing, ATLA 31:89—98
2 Библиография no объему доз
[10] HULL. R.M. Guideline limitvolumes for dosing animats In the prectimcal stage ofsafety evaluation. Human and Envi
ronmental Toxicology. 1995.14. pp. 305—307
[II] DERELANKO. M.J. and HOLLINGER. M.A. CRC Handbook of Toxicology. CRC Press. NY. 2nd edition. 2001. p. 98
[12] DIEHL. K.-H.etal.Agood practice guideto theadmmlstration ofsubstancesandremovalofblood, including routes and
volumes. J. Applied Toxicology. 21.2001. pp. 15— 23
[13] MORTON. D. etal. Effects of infusion rates in rats receiving repeated large volumes of intravenous saline solution.
Laboratory Animal Sciences. 47.1997. pp. 656—659
[14] RICHMOND. J.D. Dose limit volumes: The United Kingdom view — past and present. Presented at the Humane
Society of the United States — Refinement in Toxicology Testing Dosing Data: Volume and Freguency. March 14.
1999. New Orleans. LA
[15] MORTON. D B.etal. Refining procedures for the administration of substances. Report of the BVAAWF/FRAME/
RSPCAAJFAW Joint Working Group on Refinement. LaboratoryAnimals. 35. 2001. pp. 1—41
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