Regulations.gov document

Use of Standards in FDA Regulatory Oversight of Next Generation Sequencing (NGS)-Based In…

Other · FDA-2016-D-1270 · posted Jul 14, 2016

Key facts

Document ID FDA-2016-D-1270-0002
Title Use of Standards in FDA Regulatory Oversight of Next Generation Sequencing (NGS)-Based In Vitro Diagnostics (IVDs) Used for Diagnosing Germline Diseases Draft Guidance for Stakeholders and Food and Drug Administration Staff
Document type Other
Subtype Guidance
Agency FDA
Docket FDA-2016-D-1270
Posted Jul 14, 2016
Comment period opens Jul 14, 2016
Comments due Oct 7, 2016

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