Regulations.gov document

Guidance for Industry on Postmarketing Studies and Clinical Trials; Availability…

Notice · FDA-2009-D-0283 · posted Apr 1, 2011

Key facts

Document ID FDA-2009-D-0283-0020
Title Guidance for Industry on Postmarketing Studies and Clinical Trials; Availability: Implementation of Section 505(o)(3) of the Federal Food, Drug, and Cosmetic Act
Document type Notice
Subtype NAD-Notice of Availability of Data
Agency FDA
Docket FDA-2009-D-0283
Posted Apr 1, 2011
Federal Register citation 76 FR 18226
FR document number 2011-07707
Comment period opens Apr 1, 2011
Effective date Apr 1, 2011

At a glance

  • 1–9 Pages
  • 10–99 Public comments on this docket

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About Regulations.gov documents

Regulations.gov holds the rulemaking and other documents federal agencies post for public comment. Only agency documents are published here; public submissions are not.

Source: Regulations.gov (U.S. General Services Administration eRulemaking Program) · Source date:

Browse all Regulations.gov documents