Regulations.gov document

Guidance for Industry on Providing Regulatory Submissions in Electronic Format Orphan-Drug…

Notice · FDA-2006-D-0159 · posted Apr 6, 2006

Key facts

Document ID FDA-2006-D-0159-0001
Title Guidance for Industry on Providing Regulatory Submissions in Electronic Format Orphan-Drug and Humanitarian Use Device Designation Requests and Related Submissions
Document type Notice
Subtype NAD-Notice of Availability of Data
Agency FDA
Docket FDA-2006-D-0159
Posted Apr 6, 2006
Comment period opens Mar 31, 2006
Comments due May 31, 2006

At a glance

  • None Pages
  • No Open for comment
  • 1–9 Public comments on this docket

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

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