The Code of Federal Regulations Title 21 contains the codified Federal laws and regulations that are in effect as of the date of the publication pertaining to food and drugs, both legal pharmaceuticals and illegal drugs.

The Code of Federal Regulations is a codification of the general and permanent rules published in the Federal Register by the Executive departments and agencies of the United States Federal Government. This print ISBN is currently the Official U.S. Federal Government edition of this product. Title 21 CFR, Parts 1-99, includes rules, regulations, procedures and administrative procedures associated with the Food and Drug Administration and the Department of Health and Human Services (administrative practices, electronic records, public hearings), environmental impact considerations, pharmaceutical good manufacturing practice reports, medical device quality system audit reports/device product evaluation reports (in the United States and European community), protection of human subjects, financial disclosure by clinical investigators, good laboratory practice, patent term restoration, color additives, and more.. Related products: Investigational New Drug Application (Green Paper Folder) is available here: https://bookstore.gpo.gov/products/investigational-new-drug-application-green-paper-folder New Drug Application: Biologic Licensing Application, Archival Copy (Blue Polyethylene Folder) is available here: https://bookstore.gpo.gov/products/new-drug-application-biologic-licensing-application-archival-copy-blue-polyethylene-folder New Drug Application: Chemistry Section (Red Paper Folder) is available here: https://bookstore.gpo.gov/products/new-drug-application-chemistry-section-red-paper-folder New Drug Application: Clinical Data Section, (Tan Paper Folder) is available here: https://bookstore.gpo.gov/products/new-drug-application-clinical-data-section-tan-paper-folder New Drug Application: Pharmacology Section (Yellow Paper Folder) is available here: https://bookstore.gpo.gov/products/new-drug-application-pharmacology-section-yellow-paper-folder New Drug Application: Pharmacokinetic Section (Orange Paper Folder) is available here: https://bookstore.gpo.gov/products/new-drug-application-pharmacokinetic-section-orange-paper-folder A Legacy of Lessons Learned: Landstuhl Regional Medical Center During Wartime, 2001-2014 --Hardcover format --is available here: https://bookstore.gpo.gov/products/legacy-lessons-learned-landstuhl-regional-medical-center-during-wartime-2001-2014 --ePub format is available for immediate download for $9.99 from Apple iBookstore, Google Play eBookstore, Barnes and Noble Nook Bookstore, Overdrive, EBSCOhost, and ProQuest databases. Please use ISBN: 9780160937385 to purchase and download from these platforms.

Special edition of the Federal register. Subject/agency index for rules codified in the Code of Federal Regulations, revised as of Jan. 1 ...

The Code of Federal Regulations Title 21 contains the codified Federal laws and regulations that are in effect as of the date of the publication pertaining to food and drugs, both legal pharmaceuticals and illegal drugs.

The Code of Federal Regulations Title 21 contains the codified Federal laws and regulations that are in effect as of the date of the publication pertaining to food and drugs, both legal pharmaceuticals and illegal drugs.

The Code of Federal Regulations Title 21 contains the codified Federal laws and regulations that are in effect as of the date of the publication pertaining to food and drugs, both legal pharmaceuticals and illegal drugs.

The Code of Federal Regulations Title 21 contains the codified Federal laws and regulations that are in effect as of the date of the publication pertaining to food and drugs, both legal pharmaceuticals and illegal drugs.

The Code of Federal Regulations Title 21 contains the codified Federal laws and regulations that are in effect as of the date of the publication pertaining to food and drugs, both legal pharmaceuticals and illegal drugs.

The Code of Federal Regulations Title 21 contains the codified Federal laws and regulations that are in effect as of the date of the publication pertaining to food and drugs, both legal pharmaceuticals and illegal drugs.