This electronic document was downloaded from the GPO web site, September 2002, and is provided for information purposes only. The Code of Federal Regulations, Title 21, is updated each year in early summer. The most current version of the regulations may be found at the GPO web site or from the current printed version.

[Code of Federal Regulations]
[Title 21, Volume 1]
[Revised as of April 1, 2002]
From the U.S. Government Printing Office via GPO Access
[CITE: 21CFR58.41]
 
[Page 313]
 
                        TITLE 21--FOOD AND DRUGS
 
CHAPTER I--FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN
                                SERVICES
 
PART 58--GOOD LABORATORY PRACTICE FOR NONCLINICAL LABORATORY STUDIES--Table of Contents
 
                          Subpart C--Facilities
 
Sec. 58.41  General.
 
 
    Each testing facility shall be of suitable size and construction to
facilitate the proper conduct of nonclinical laboratory studies. It
shall be designed so that there is a degree of separation that will
prevent any function or activity from having an adverse effect on the
study.
 
[52 FR 33780, Sept. 4, 1987]


Guidance Documents for Submitting Petitions
Foods Home   |   FDA Home   |   Search/Subject Index   |   Disclaimers & Privacy Policy   |   Accessibility/Help