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Vol 23 No 5 May/June 2018

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Drafting Commercial Agreements

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Code of Federal Regulations: Title 21: Food and Drugs Parts 600-799, Revised as of April 1, 2002

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ISBN13: 9783805575256
ISBN: 3805575254
Published: September 2002
Publisher: Karger
Format: Paperback
Price: POA

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.

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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.