Changeflow GovPing Healthcare FDA Acknowledgement Letter to Charlene Peters
Routine Notice Added Final

FDA Acknowledgement Letter to Charlene Peters

Favicon for www.regulations.gov Regs.gov: Food and Drug Administration
Published March 27th, 2026
Detected March 28th, 2026
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Summary

The Food and Drug Administration (FDA) has issued an acknowledgement letter to Charlene Peters regarding a submission. The letter, authored by CDER, confirms receipt of the document. No specific details about the submission's content or regulatory implications are provided.

What changed

This document is an acknowledgement letter from the FDA's Division of Management and Budget (DMB) to Charlene Peters, confirming receipt of a submission. The letter, authored by CDER, is noted as containing restricted personally identifiable information in its original form, with a redacted version also available. The purpose of this notice is purely administrative, confirming that a submission has been received by the agency.

For regulated entities, this notice signifies that a submission has entered the FDA's processing system. As it is merely an acknowledgement, it does not indicate approval, disapproval, or any specific action required from the recipient or other parties. Compliance officers should note that this is a standard procedural communication and does not impose new obligations or require immediate action beyond what may have already been submitted.

Source document (simplified)

Content

There are no documents available to view or download

Attachments 2

Acknowledgement Letter from FDA DMB to Charlene Peters

Restricted: Personally Identifiable Information

More Information
- Author(s) CDER

Acknowledgement Letter from FDA DMB to Charlene Peters - Redacted

More Information
- Author(s) CDER
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Classification

Agency
FDA
Published
March 27th, 2026
Instrument
Notice
Legal weight
Non-binding
Stage
Final
Change scope
Minor
Document ID
FDA-2026-P-3169-0002
Docket
FDA-2026-P-3169

Who this affects

Applies to
Drug manufacturers Medical device makers
Industry sector
3254 Pharmaceutical Manufacturing 3345 Medical Device Manufacturing
Geographic scope
United States US

Taxonomy

Primary area
Healthcare
Operational domain
Compliance
Compliance frameworks
FDA 21 CFR Part 11
Topics
Pharmaceuticals Medical Devices

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