Superseded
, Reaffirmed
Standard
Historical
ASTM E1298-89(2000)
Standard Guide for Determination of Purity, Impurities, and Contaminants in Biological Drug Products
Summary
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:
| Section | |
| Terminology | 2 |
| Significance and Use | 3 |
| Purity | 4 |
| General Considerations | 4.1 |
| Estimation of Purity | 4.2 |
| Impurities | 5 |
| General Considerations | 5.1 |
| Major and Minor | 5.2 |
| Nature and Consequences of | 5.3 |
| Contaminants | 6 |
| General Considerations | 6.1 |
| Effects of contaminants | 6.2 |
| Methods for Determining Impurities and Contaminants | 7 |
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.
Technical characteristics
| Publisher | American Society for Testing and Materials (ASTM International) |
| Publication Date | 01/01/1989 |
| Confirmation Date | 01/01/2000 |
| Collection | |
| Page Count | 3 |
| Themes | Medicaments |
| EAN | --- |
| ISBN | --- |
| Weight (in grams) | --- |
Replaces
01/01/1989
Superseded
, Reaffirmed
Historical
Previous versions
01/11/2006
Withdrawn
Most Recent
01/01/1989
Superseded
, Reaffirmed
Historical
01/01/1989
Superseded
, Reaffirmed
Historical