Telehealth regulatory actions tracker

Approvals, clearances, rules, guidance, recalls, advisory committee meetings and enforcement actions from FDA, DEA, CMS, HHS and FTC that affect telehealth, compounding, GLP-1 drugs, peptides and digital health.

No actions yet. Records appear here as soon as they are verified.

Methodology

Data sources

Federal Register — rules, proposed rules and notices
FDA press announcements
FDA recalls, market withdrawals and safety alerts
openFDA — approvals, device clearances and enforcement reports
FDA warning letters database
Regulations.gov — dockets and comment deadlines

What we include

Federal actions that change what telehealth companies, prescribers, pharmacies or patients may do, or that concern GLP-1 drugs, peptides, compounding or health AI.
Warning and untitled letters also appear in the FDA warning letters tracker, which owns their record pages.
Actions are dated by the date on the agency document; effective dates and comment deadlines are recorded separately.

How we verify

Each record links the agency’s own document, and identifiers are checked against the Federal Register, Regulations.gov or FDA databases.
Status (proposed, final, in effect, delayed, vacated) is updated when the agency or a court acts.

Known gaps

State actions are not systematically covered.
The tracker is curated for our beats; it is not a complete list of every federal action.

Update frequency: Updated as agencies publish; Federal Register and FDA postings are checked each business day.

CSV columns (27)

The CSV file is UTF-8 (with a byte-order mark for Excel), comma-separated with CRLF line endings (RFC 4180), one row per record, with these columns in order. Dates are YYYY-MM-DD (U.S. Eastern); list values are separated by semicolons.

record_url: Permanent record page on this site.
title: Record title.
action_type: Action type code (e.g. warning-letter, recall, fr-rule, approval).
agency: Issuing agency (FDA, DEA, CMS, HHS, FTC, DOJ, state-board, other).
issued_date: Date on the document (YYYY-MM-DD, U.S. Eastern).
posted_date: Date the agency posted it publicly, when different.
effective_date: Effective date (rules and policy changes).
comments_close_date: Public comment deadline (proposed rules).
status: Record status code (open, proposed, final, effective, delayed, vacated, closed-out).
recipient: Company or organization the action names (letters, recalls, approvals).
recipient_url: Profile page of the recipient on this site.
subject: Short product or company label.
products: Drugs and peptides named in the action, separated by semicolons.
subjects: Violation or topic categories, separated by semicolons.
status_labels: Status Label codes shown on the page, separated by semicolons.
fr_document_number: Federal Register document number.
docket_id: Regulations.gov docket ID.
rin: Regulation Identifier Number.
recall_number: FDA recall event number.
recall_class: FDA recall class (I, II or III).
source_url: The agency’s own document.
archived_url: Our archived copy of the document, when available.
company_response: Public company response, as summarized by our staff.
company_response_url: Link to the company’s response.
closeout_date: Date of the agency’s close-out letter, if any.
summary: Staff-written plain-English summary (blank until written).
last_updated: When this record last changed (ISO 8601).