You are here
Australian code of good manufacturing practice for human blood and blood components, human tissues and human cellular therapy products
V1.0, April 2013
- Australian Code of Good Manufacturing Practice – Human Blood and Tissues. 2000. TGA.
- Australian Code of good Manufacturing Practice for Medicinal Products, 2002
- Guide to the preparation, use and quality assurance of blood components. 14th ed, 2008. Council of Europe
- Recommendations on Validation Master Plan, Installation and Operation Qualification, Non-Sterile Process Validation, Cleaning Validation. PI 006-2, 1 July 2004. PIC/S.
- Guide to Good Manufacturing Practice for Medicinal Products. PE 009-5, 1 August 2006. PIC/S.
- Guide to Good Manufacturing Practice for Medicinal Products. PE 009-8 15 15 January, 2009. PIC/S