Regulations.gov document

Draft Guidance for Industry and Review Staff on Nonclinical Safety Evaluation of…

Other · FDA-2008-D-0142 · posted Mar 7, 2008

Key facts

Document ID FDA-2008-D-0142-0002
Title Draft Guidance for Industry and Review Staff on Nonclinical Safety Evaluation of Reformulated Drug Products and Products Intended for Administration by an Alternate Route; Guidance Document
Document type Other
Subtype GDL-Guidance (Supporting and Related Materials)
Agency FDA
Docket FDA-2008-D-0142
Posted Mar 7, 2008
Comment period opens Mar 7, 2008
Comments due May 7, 2008

At a glance

  • No Open for comment
  • 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