1.1 This guide is applicable to all elements of pharmaceutical and biopharmaceutical manufacturing systems including: good manufacturing practice (GMP) utility equipment, process equipment, supporting utilities, associated process monitoring and control systems, and automation systems that have the potential to affect product quality and patient safety.
Product Details
- Published:
- 10/01/2020
- Number of Pages:
- 6
- File Size:
- 1 file , 110 KB
- Redline File Size:
- 2 files , 230 KB
