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Test Method Protocol for Solubility Determination (2003)

Test Method Protocol for Solubility Determination Phase III - Validation Study September 24, 2003 TEST Method Protocol for Solubility Determination In Vitro Cytotoxicity Validation Study Phase III September 24, 2003 Prepared by The National Toxicology Program (NTP) Interagency Center for the Evaluation of Alternative Toxicological Methods (NICEATM) Based on Standard Operating Procedure Recommendations from an International Workshop Organized by the Interagency Coordinating Committee on the Validation of Alternative Methods (ICCVAM) National Institute of Environmental Health Sciences (NIEHS) National Institutes of Health (NIH) Public Health Service Department of Health and Human Services 1 Test Method Protocol for Solubility Determination Phase III - Validation Study September 24, 2003 TEST Method Protocol Solubility Determination Phase III I. PURPOSE The purpose of this study is to evaluate the cytotoxicity of test chemicals using the BALB/c 3T3 Neutral Red Uptake (NRU) and normal human keratinocyte (NHK) cytotoxicity tests.

Test Method Protocol for Solubility Determination Phase III - Validation Study September 24, 2003 . TEST METHOD PROTOCOL. Solubility Determination Phase III. I. PURPOSE . The purpose of this study is to evaluate the cytotoxicity of test chemicals using the BALB/c 3T3 Neutral Red Uptake (NRU) and normal human keratinocyte (NHK) cytotoxicity tests.

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