Code of Federal Regulations: Food and Drugs, Parts 200 to 299

Code of Federal Regulations: Food and Drugs, Parts 200 to 299

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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 manufactures, which also pertains to blood banking establishments. This section addresses current good manufacturing practice requirements for the manufacturing, processing, packing or holding of drug products and current good manufacturing practice requirements for finished pharmaceuticals. Included in this section of the regulations are requirements for a quality control unit.show more

Product details

  • Paperback | 200 pages
  • S Karger Ag
  • American Association of Blood Banks
  • Basel, Switzerland
  • 3805576285
  • 9783805576284

Table of contents

Finding aids material 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