[Code of Federal Regulations]
[Title 21, Volume 1]
[Revised as of April 1, 2003]
From the U.S. Government Printing Office via GPO Access
[CITE: 21CFR5.35]

[Page 47]
 
                        TITLE 21--FOOD AND DRUGS
 
CHAPTER I--FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN 
                                SERVICES
 
PART 5--DELEGATIONS OF AUTHORITY AND ORGANIZATION--Table of Contents
 
              Subpart B--General Redelegations of Authority
 
Sec. 5.35  Officials authorized to make certification under 5 U.S.C. 605(b) for any proposed and final rules.

    (a) The following officials are authorized to perform all the 
functions of the Commissioner of Food and Drugs with regard to decisions 
made under the Regulatory Flexibility Act (5 U.S.C. 605(b)), to certify 
that a proposed or final rule, if issued, will not have a significant 
economic impact on a substantial number of small entities:
    (1) The Associate Commissioner for Regulatory Affairs.
    (2) The Director, Center for Biologics Evaluation and Research.
    (3) The Director, Center for Drug Evaluation and Research.
    (4) The Director, Center for Devices and Radiological Health.
    (5) The Director, Center for Food Safety and Applied Nutrition.
    (6) The Director, Center for Veterinary Medicine.
    (7) Other Food and Drug Administration Officials authorized to issue 
Federal Register documents.
    (b) These officials may not further redelegate this authority.