[Code of Federal Regulations]
[Title 21, Volume 1]
[Revised as of April 1, 2001]
From the U.S. Government Printing Office via GPO Access
[CITE: 21CFR5.25]

[Page 37-38]
 
                        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--Redelegations of Authority from the Commissioner of Food and 
                                  Drugs
 
Sec. 5.25  Research, investigation, and testing programs and health information and health promotion programs.

    (a) The following officials are authorized under sections 301, 307, 
311, 1701, 1702, 1703, and 1704 of the Public Health Service Act (the 
act) to establish research, investigation, and testing programs and 
health information and health promotion programs, which relate to their 
assigned functions, and to approve grants for conducting such programs:
    (1) The Director and Deputy Director, National Center for 
Toxicological Research.
    (2) The Director and Deputy Directors, Centers for Devices and 
Radiological Health (CDRH).

[[Page 38]]

    (3) The Director and Deputy Director, Center for Biologics 
Evaluation and Research.
    (4) The Director and Deputy Directors, Center for Food Safety and 
Applied Nutrition.
    (5) The Director and Deputy Director, Center for Veterinary 
Medicine.
    (6) The Director, Deputy Center Director for Review Management, and 
Deputy Center Director for Pharmaceutical Science, Center for Drug 
Evaluation and Research (CDER).
    (7) The Director, Office of Orphan Products Development, Office of 
the Senior Associate Commissioner, Office of the Commissioner.
    (b) The Director and Deputy Directors, CDRH, are authorized to 
establish an electronic product radiation control program and to approve 
grants for conducting the program under section 356 of the Act.
    (c) The Deputy Commissioner for Management and Systems, Office of 
Management and Systems, Office of the Commissioner; the Director and 
Deputy Director, Office of Facilities, Acquisitions, and Central 
Services, Office of Management and Systems, Office of the Commissioner; 
the Director, Division of Contracts and Procurement Management, Office 
of Facilities, Acquisitions, and Central Services, Office of Management 
and Systems, Office of the Commissioner; and the Chief Grants Management 
Officer and the Grants Management Officer, Division of Contracts and 
Procurement Management, Office of Facilities, Acquisitions, and Central 
Services, Office of Management Systems, Office of the Commissioner are 
authorized to sign and issue all notices of grant awards and amendments 
thereto and sign and issue notices of suspension and termination thereof 
for grants approved under the authority delegated in paragraphs (a) and 
(b) of this section.
    (d) The Director of the National Center for Toxicological Research 
is authorized under section 301, as amended by Pub. L. 95-622, of the 
Public Health Service Act to make available to educational institutions, 
for biomedical and behavioral research, laboratory animals bred for 
research purposes of the Center which are not required to support Center 
research programs.

[45 FR 7783, Feb. 5, 1980, as amended at 45 FR 27924, Apr. 25, 1980; 46 
FR 17758, Mar. 20, 1981; 48 FR 56946, Dec. 27, 1983; 49 FR 14932, 14936, 
Apr. 16, 1984; 50 FR 4859, Feb. 4, 1985; 54 FR 8316, Feb. 28, 1989; 57 
FR 45295, Oct. 1, 1992; 59 FR 42491, Aug. 18, 1994; 62 FR 2554, Jan. 17, 
1997; 62 FR 67270, Dec. 24, 1997; 65 FR 34962, June 1, 2000]