Abstract
The mission of achieving good manufacturing practice (GMP) license for the drugs production is to ensure the quality and efficacy of pharmaceutical products, thus assure the public safety. Compliance of GMP standard can increase the competitiveness, efficiency of production, images for pharmaceutical manufacturing firms against international market development. In meeting these ends pharmaceutical firms must assure that the manufacturing processes, verifications of the end products validations of the manufacturing processes and equipment as well as the inspection equipment and procedures are properly conducted with a proper documentation system. The authors will focus on the strategic implementation of GMP.
| Original language | English |
|---|---|
| Title of host publication | Quality Management |
| Subtitle of host publication | A New Era: Hong Kong, 14-15 January 2005 |
| Pages | 38-50 |
| Number of pages | 13 |
| ISBN (Electronic) | 9789812701930 |
| DOIs | |
| Publication status | Published - 1 Jan 2005 |
Fingerprint
Dive into the research topics of 'A road map to good manufacturing practice'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver