Code of Federal Regulations: Title 21: Food and Drugs Parts 600-799, Revised as of April 1, 2002
This section of the "Code of Federal Regulations" codifies the general and permanent rules established by the Food and Drug Administration (FDA) that pertain to whole blood and blood products. This section addresses FDA registration and licensure requirements for establishments, personnel requirements, record keeping, labelling, good manufacturing practice and additional specific requirements for whole blood and blood products.
- Paperback | 194 pages
- 24 Sep 2002
- S Karger Ag
- American Association of Blood Banks
- Basel, Switzerland
Table of contents
Explanation. title 21: chapter I Food and Drug Administration, Department of Health and Human Services (continued). Finding Aids: material approved for incorporation by reference; table of CFR titles and chapters; alphabetical lists of agencies appearing in the CFR; list of CFR sections offered.