[Code of Federal Regulations]
[Title 21, Volume 4]
[Revised as of April 1, 2007]
From the U.S. Government Printing Office via GPO Access
[CITE: 21CFR203.2]
[Page 100-101]
TITLE 21--FOOD AND DRUGS
CHAPTER I--FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN
SERVICES (CONTINUED)
PART 203 PRESCRIPTION DRUG MARKETING--Table of Contents
Subpart A General Provisions
Sec. 203.2 Purpose.
The purpose of this part is to implement the Prescription Drug
Marketing Act of 1987 and the Prescription Drug
[[Page 101]]
Amendments of 1992, except for those sections relating to State
licensing of wholesale distributors (see part 205 of this chapter), to
protect the public health, and to protect the public against drug
diversion by establishing procedures, requirements, and minimum
standards for the distribution of prescription drugs and prescription
drug samples.
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