Code of Federal Regulations, Title 21, Food and Drugs, Parts 800 to 1299 : Revised as of April 1, 2006
This section contains the current good manufacturing practice regulations for medical devices that have been revised and incorporated into quality system regulations for medical devices. It is particularly relevant to blood bank computer systems. Also included are the regulations for good tissue practice for human cells, tissues, and cellular and tissue based products that are included in part 1271, and for human tissue intended for transplantation (part 1270).
- Paperback | 786 pages
- 27 Nov 2006
- S Karger Ag
- Basel, Switzerland