Regulations.gov document

09 Reference 8 FDA Guidance for Industry Availability of FDAs e_Submitter Program for…

Supporting & Related Material · FDA-2016-D-4308 · posted Dec 21, 2018

Key facts

Document ID FDA-2016-D-4308-0031
Title 09 Reference 8 FDA Guidance for Industry Availability of FDAs e_Submitter Program for Regulatory Submissions from Licensed Blood Establishments August 2011
Document type Supporting & Related Material
Subtype Background Material
Agency FDA
Docket FDA-2016-D-4308
Posted Dec 21, 2018

At a glance

  • 1–9 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