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. CFR 21 covers pharmaceutical goods manufacturing reports, medical device quality system audit reports, and certain medical device product evaluation reports, plus patent term restoration, color additives certifications, dissemination of information on unapproved/new uses for marketed drugs, biologics, and devices, and more. , Medical device manufacturers, pharmaceutical manufacuters, physicians, hospital administrators and technicians may be interested in this volume. Additionally, medical school students, and med student interns may also be interested to be updated on the latest regulations relating to pharma and device manufacturers.