[Code of Federal Regulations]
[Title 21, Volume 1]
[Revised as of April 1, 2007]
From the U.S. Government Printing Office via GPO Access
[CITE: 21CFR20.105]
[Page 213]
TITLE 21--FOOD AND DRUGS
CHAPTER I--FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN
SERVICES
PART 20 PUBLIC INFORMATION--Table of Contents
Subpart F Availability of Specific Categories of Records
Sec. 20.105 Testing and research conducted by or with funds provided by the
Food and Drug Administration.
(a) Any list that may be prepared by the Food and Drug
Administration of testing and research being conducted by or with funds
provided by the Food and Drug Administration is available for public
disclosure.
(b) Any contract relating to agency testing and research, and any
progress report relating thereto, is available for public disclosure.
(c) The results of all testing or research conducted by or with
funds provided by the Food and Drug Administration, such as
toxicological testing, compliance assays, methodology studies, and
product testing, are available for public disclosure when the final
report is complete and accepted by the responsible Food and Drug
Administration official, after deletion of any information that would
reveal confidential investigative techniques and procedures, e.g., the
use of ``markers'' to document adulteration of a product. If such
results are disclosed in an authorized manner to any member of the
public before the final report is available, they are immediately
available for public disclosure to any member of the public who requests
them.
(d) Access to all raw data, slides, worksheets, and other similar
working materials shall be provided at the same time that the final
report is disclosed.
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