[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: 21CFR226.10]

[Page 146]
 
                        TITLE 21--FOOD AND DRUGS
 
CHAPTER I--FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN 
                          SERVICES (CONTINUED)
 
PART 226--CURRENT GOOD MANUFACTURING PRACTICE FOR TYPE A MEDICATED ARTICLES--Table of Contents
 
                      Subpart A--General Provisions
 
Sec. 226.10  Personnel.

    The key personnel and any consultants involved in the manufacture 
and control of the Type A medicated article(s) shall have a background 
of appropriate education or appropriate experience or combination 
thereof for assuming responsibility to assure that the Type A medicated 
article(s) has the proper labeling and the safety, identity, strength, 
quality, and purity that it purports to possess.