Spiral-bound, 5.5" x 8.5" version of the Code of Federal Regulations, Title 21: Food and Drugs, Parts 200-299, April 1, 2020, previously available only from the Government Printing Office. 214 pages.
This book is for pharmaceutical industry and health care professionals who want hard-copy access to all of the food and drug regulations in parts 200-299.
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• 1-249 copies: $20.00 • 250-499 copies: 19.00
• 500-749 copies: $18.00 • 750+ copies: $17.00
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• 1-24 copies: unavailable • 25-100 copies: $2.00/book
• 100-249 copies: $1.00/book • 250+ copies: No charge
* Based on quantities of a single book title
• CFR Title 21: Food and Drugs (Revised as of April 1, 2020)
202 Prescription Drug Advertising
203 Prescription Drug Marketing
205 Guidelines for State Licensing of Wholesale Prescription Drug
206 Imprinting of Solid Oral Dosage Form Drug Products for
207 Requirements for Foreign and Domestic Establishment
Registration and Listing for Human Drugs, Including Drugs that
are Regulated Under a Biologics License Application, and
Animal Drugs, and the National Drug Code
208 Medication Guides for Prescription Drug Products
209 Requirement for Authorized Dispensers and Pharmacies to
Distribute a Side Effects Statement
210 Current Good Manufacturing Practice in Manufacturing,
Processing, Packing, or Holding of Drugs; General
211 Current Good Manufacturing Practice for Finished
212 Current Good Manufacturing Practice for Positron Emission
216 Human Drug Compounding
225 Current Good Manufacturing Practice for Medicated Feeds
226 Current Good Manufacturing Practice for Type A Medicated
250 Special Requirements for Specific Human Drugs
290 Controlled Drugs
299 Drugs; Official Names and Established Names
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