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- Title
WHO GOOD MANUFACTURING PRACTICES FO R EXCIPIENTS USED IN PHARMACEUTICAL PRODUCTS.
- Abstract
The article explains the WHO's Good Manufacturing Practices (GMP) guidelines for pharmaceutical excipients. It emphasizing the importance of maintaining quality and safety throughout the production, control, storage and distribution of excipients used in pharmaceutical products; the risks associated with using excipients that may contain impurities; underlines the need for an established quality management system to mitigate risks; and the reliability of excipients throughout the supply chain.
- Subjects
WORLD Health Organization; MANUFACTURING industries; QUALITY assurance; QUALITY control; INFORMATION resources; PHARMACY information services; PHARMACEUTICAL industry; GENETIC techniques; MANAGEMENT; DOSAGE forms of drugs
- Publication
WHO Drug Information, 2023, Vol 37, Issue 2, p278
- ISSN
1010-9609
- Publication type
Article