(a) DefinitionIn this section, the term “article” means a paper, poster, abstract, book, book chapter, or other published writing.
(b) PoliciesThe Secretary, through the Commissioner of Food and Drugs, shall establish and make publicly available clear written policies to implement this section and govern the timely submission, review, clearance, and disclaimer requirements for articles.
(c) Timing of submission for reviewIf an officer or employee, including a Staff Fellow and a contractor who performs staff work, of the Food and Drug Administration is directed by the policies established under subsection (b) to submit an article to the supervisor of such officer or employee, or to some other official of the Food and Drug Administration, for review and clearance before such officer or employee may seek to publish or present such an article at a conference, such officer or employee shall submit such article for such review and clearance not less than 30 days before submitting the article for publication or presentation.
(d) Timing for review and clearanceThe supervisor or other reviewing official shall review such article and provide written clearance, or written clearance on the condition of specified changes being made, to such officer or employee not later than 30 days after such officer or employee submitted such article for review.
(e) Non-timely reviewIf, 31 days after such submission under subsection (c), the supervisor or other reviewing official has not cleared or has not reviewed such article and provided written clearance, such officer or employee may consider such article not to have been cleared and may submit the article for publication or presentation with an appropriate disclaimer as specified in the policies established under subsection (b).
(f) EffectNothing in this section shall be construed as affecting any restrictions on such publication or presentation provided by other provisions of law.
Structure US Code
CHAPTER 9— FEDERAL FOOD, DRUG, AND COSMETIC ACT
SUBCHAPTER VII— GENERAL AUTHORITY
Part A— General Administrative Provisions
§ 371. Regulations and hearings
§ 372. Examinations and investigations
§ 374a. Inspections relating to food allergens
§ 376. Examination of sea food on request of packer; marking food with results; fees; penalties
§ 379. Confidential information
§ 379a. Presumption of existence of jurisdiction
§ 379b. Consolidated administrative and laboratory facility
§ 379d. Automation of Food and Drug Administration
§ 379d–1. Conflicts of interest
§ 379d–2. Policy on the review and clearance of scientific articles published by FDA employees
§ 379d–3. Streamlined hiring authority
§ 379d–3a. Hiring authority for scientific, technical, and professional personnel
§ 379d–3b. Strategic Workforce Plan and report
§ 379d–4. Reporting requirements
§ 379d–5. Guidance document regarding product promotion using the Internet