[Code of Federal Regulations]
[Title 21, Volume 4]
[Revised as of April 1, 2003]
From the U.S. Government Printing Office via GPO Access
[CITE: 21CFR210.2]

[Page 115]
 
                        TITLE 21--FOOD AND DRUGS
 
CHAPTER I--FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN 
                          SERVICES (CONTINUED)
 
PART 210--CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PROCESSING, PACKING, OR HOLDING OF DRUGS; GENERAL--Table of Contents
 
Sec. 210.2  Applicability of current good manufacturing practice regulations.

    (a) The regulations in this part and in parts 211 through 226 of 
this chapter as they may pertain to a drug and in parts 600 through 680 
of this chapter as they may pertain to a biological product for human 
use, shall be considered to supplement, not supersede, each other, 
unless the regulations explicitly provide otherwise. In the event that 
it is impossible to comply with all applicable regulations in these 
parts, the regulations specifically applicable to the drug in question 
shall supersede the more general.
    (b) If a person engages in only some operations subject to the 
regulations in this part and in parts 211 through 226 and parts 600 
through 680 of this chapter, and not in others, that person need only 
comply with those regulations applicable to the operations in which he 
or she is engaged.