Code of Federal Regulations: Title 21: Food and Drugs, Parts 200 - 299 - Revised as of April 1, 2001

Code of Federal Regulations: Title 21: Food and Drugs, Parts 200 - 299 - Revised as of April 1, 2001

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Description

This section of the "Code of Federal Regulations" codifies the general and permanent rules established by the Food and Drug Administration (FDA) for prescription drug manufacturers, which also pertains to blood banking establishments. This section addresses good manufacturing practice requirements for the manufacturing, processing, packing, or holding of drug products, and good manufacturing practice requirements for finished pharmaceuticals from 2001. Included in this section of the regulations are requirements for a quality control unit.show more

Product details

  • Paperback | 218 pages
  • S Karger Ag
  • American Association of Blood Banks
  • Basel, Switzerland
  • 3805573987
  • 9783805573986

Table of contents

Explanation; title 21, chapter 1 - food and drug administration, department of health and human services (continued); finding aids 0 materila approved for incorporation by reference; table of CFR titles and chapters; alphabetical list of agencies appearing in the CFR; list of CFR sections affected.show more