Cfr Title 21

Written by Rylee Newton
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If you're looking for a resource for CFR Title 21, you probably have a specific research goal in mind. When it comes to government publications like this one, you will find very detailed information regarding rules and regulations that govern the Food and Drug Administration and the Department of Health and Human Services. This is a useful reference tool for a number of different industries including many different branches of health and pharmaceutical related fields.

CFR Title 21 comes as a nine-volume set or you can purchase the individual volume that deals with your specific area of interest. Many companies are affected by the decisions and policies of these two government agencies. The information contained in this set is invaluable in making budgetary decisions, effecting policy changes, and establishing research and development priorities.

Information Contained in CFR Title 21

CFR Title 21 provides companies and individuals with a set of guidelines that must be met in order to comply with federal standards. This title is just one of the 50 titles available from the Government Printing Office called the Code of Federal Regulations. Title 21 is a comprehensive list of regulations from the Food and Drug Administration, the Drug Enforcement Administration, and the National Drug Control Agency.

This title addresses products that are made for human and animal consumption and also governs that production of medical devices, cosmetics, radiological health, and controlled substances. The Code of Federal Regulations prints title on a quarterly basis. Annual changes to Title 21 must be posted by the FDA, the DEA and the NDCA by April. You can log onto the Internet for specific publishing dates, and for resources for purchasing this title.


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