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FDA Variance Approval Letter to DJ Ken-E. Ken

The Food and Drug Administration (FDA) has posted a Variance Approval Letter related to DJ Ken-E. Ken. The document was issued by the Center for Devices and Radiological Health (CDRH). No other details or documents are available for viewing.

Routine Notice Healthcare
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FDA Variance Application from Jennifer Rishel

The FDA has posted a variance application submitted by Jennifer Rishel. The application, filed by CDRH, is available in redacted format on regulations.gov. No specific details on the nature of the variance or its implications are provided in the posting.

Routine Notice Healthcare
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FDA Completeness Assessment Correspondence

The FDA has issued a completeness assessment correspondence to Hyman, Phelps & McNamara, P.C. regarding a submission. The document is a standard communication within the drug approval process and does not contain new regulatory requirements or guidance.

Routine Notice Pharmaceuticals
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FDA Variance Application from Kenyon Productions, LLC Closed

The Food and Drug Administration (FDA) has closed a variance application submitted by Kenyon Productions, LLC. The specific details of the variance and the reasons for its closure are not provided in the available document.

Routine Notice Healthcare
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FDA Variance Application from JSMJ Group LLC

The FDA has received a variance application from JSMJ Group LLC. The application pertains to medical device regulations. No documents are currently available for viewing or download.

Routine Guidance Healthcare
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FDA Letter to Patent Office

The Food and Drug Administration (FDA) has issued a letter to the U.S. Patent and Trademark Office (USPTO). This communication is related to the Center for Drug Evaluation and Research (CDER) and is part of the FDA's ongoing regulatory processes. The comment period for this notice has closed.

Routine Notice Pharmaceuticals
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FDA Letter to U.S. Patent Office

The Food and Drug Administration (FDA) has issued a letter to the U.S. Patent and Trademark Office. The letter is authored by CDER and was posted on March 19, 2026. No documents are available for viewing or download.

Routine Notice Intellectual Property
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FDA Letter to U.S. Patent and Trademark Office

The Food and Drug Administration (FDA) has posted a letter addressed to the U.S. Patent and Trademark Office. The document is available on Regulations.gov and was authored by the Center for Drug Evaluation and Research (CDER).

Routine Notice Pharmaceuticals
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FDA Variance Application - Furew Floral Event and Landscaping

The Food and Drug Administration (FDA) has received a variance application from Furew Floral Event and Landscaping. The application, submitted by CDRH, is available for review on Regs.gov.

Routine Guidance Healthcare
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FDA Complaint Filed

The FDA has filed a complaint regarding a matter related to its regulatory oversight. The document indicates that comments were closed on March 19, 2026. No specific details about the complaint's nature or the parties involved are available in the provided metadata.

Routine Enforcement Healthcare

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