Business · 01/04/2011Updated: 10/17/2026 · 1 min read

FDA Reopens Comment Period for Molecular and Clinical Genetics Panel Meeting

Summary

The FDA is extending the public comment period for the Molecular and Clinical Genetics Panel meeting until May 2, 2011, to gather updated information and new comments on direct-to-consumer genetic tests making medical claims.

Original source language: Federal Register — Health and Human ServicesOpen original release →

Add your company to Business Communicator

We monitor business sources and connect attention with companies, profiles and services available in Business Communicator.

Create a free company profile Explore businesses on Business Maps →

Create a free company profile →

Explore insights

Business insights →

Global Markets News Trade Regulation News Business Technology News Fintech for Business: Payments & Banking News Supply Chain News Central Bank Policy News

Related business signals

Business · 9/14/2026

CMS Invites Public Comment on Proposed Information Collection

The Centers for Medicare & Medicaid Services (CMS) is seeking public input on its plan to gather information from the public, as required by the Paperwork Reduction Act of 1995, and invites comments on the proposed collection, including its necessity, accuracy, and potential uses of technology to reduce the burden.

Read summary →

Business · 9/16/2026

Microbiology Devices Panel of the Medical Devices Advisory Committee; Notice of Meeting; Establishment of a Public Docket; Request for Comments-Pathogen-Agnostic Sequencing

The Food and Drug Administration (FDA) announces a public advisory committee meeting of the Microbiology Devices Panel to discuss pathogen-agnostic sequencing for emergency preparedness and response efforts.

Read summary →

Business · 9/16/2026

Agency Information Collection Request; 30-Day Public Comment Request

The Office of the Secretary (OS), Department of Health and Human Services, submitted an Information Collection Request (ICR) to the Office of Management and Budget (OMB) for review and approval, with a 30-day public comment period.

Read summary →

Business · 9/28/2026

CDC Invites Public Comment on Proposed Data Collection for Public Health Emergency Preparedness

The Centers for Disease Control and Prevention (CDC) is seeking public input on a proposed data collection project, titled Public Health Emergency Preparedness (PHEP) Cooperative Agreement, as part of its efforts to reduce public burden and maximize the utility of government information, in accordance with the Paperwork Reduction Act of 1995.

Read summary →

Business · 9/28/2026

CDC Requests Public Comment on Proposed Colorectal Cancer Control Program Monitoring Activities

The Centers for Disease Control and Prevention (CDC) is seeking public input on a proposed data collection project, Colorectal Cancer Control Program (CRCCP) Monitoring Activities, as part of its effort to reduce public burden and maximize the utility of government information, in compliance with the Paperwork Reduction Act of 1995.

Read summary →

Business · 9/15/2026

FDA Establishes Public Docket for Rare Disease Clinical Investigations Statistical Considerations

The FDA is collecting feedback on statistical considerations for rare disease clinical investigations through a public docket, which is open until a certain date, and a Rare Disease Innovation, Science, and Exploration (RISE) Workshop on the topic.

Read summary →