[Code of Federal Regulations]
[Title 21, Volume 4]
[Revised as of April 1, 2002]
From the U.S. Government Printing Office via GPO Access
[CITE: 21CFR211.87]

[Page 124]
 
                        TITLE 21--FOOD AND DRUGS
 
CHAPTER I--FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN 
                          SERVICES (CONTINUED)
 
PART 211--CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS--Table of Contents
 
    Subpart E--Control of Components and Drug Product Containers and 
                                Closures
 
Sec. 211.87  Retesting of approved components, drug product containers, and closures.

    Components, drug product containers, and closures shall be retested 
or reexamined, as appropriate, for identity, strength, quality, and 
purity and approved or rejected by the quality control unit in 
accordance with Sec. 211.84 as necessary, e.g., after storage for long 
periods or after exposure to air, heat or other conditions that might 
adversely affect the component, drug product container, or closure.