ASTM International Standard Guide for Determination of Purity, Impurities, and Contaminants in Biological Drug Products ASTM E1298-89(2000)

Description
1.1 This guide covers the concepts of purity, impurity, and contamination in biological drug products. 1.2 This guide suggests methods for determination of impurities and contaminants in such products. 1.3 This guide is arranged as follows: 1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.
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Description
1.1 This guide covers the concepts of purity, impurity, and contamination in biological drug products. 1.2 This guide suggests methods for determination of impurities and contaminants in such products. 1.3 This guide is arranged as follows: 1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.
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Standard Guide for Determination of Purity, Impurities, and Contaminants in Biological Drug Products - ASTM E1298-89(2000) - ASTM International
West Conshohocken, PA, United States
Standard Guide for Determination of Purity, Impurities, and Contaminants in Biological Drug Products
ASTM E1298-89(2000)
Standard Guide for Determination of Purity, Impurities, and Contaminants in Biological Drug Products ASTM E1298-89(2000)
1.1 This guide covers the concepts of purity, impurity, and contamination in biological drug products. 1.2 This guide suggests methods for determination of impurities and contaminants in such products. 1.3 This guide is arranged as follows: 1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.

1.1 This guide covers the concepts of purity, impurity, and contamination in biological drug products.

1.2 This guide suggests methods for determination of impurities and contaminants in such products.

1.3 This guide is arranged as follows:

1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.

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Technical Specifications

  ASTM International
Product Category Standards and Technical Documents
Product Number ASTM E1298-89(2000)
Product Name Standard Guide for Determination of Purity, Impurities, and Contaminants in Biological Drug Products
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