Market catalog

FDA Regulatory Change Monitor

A proposed public regulatory data feed for product, compliance, and research teams tracking recalls, enforcement reports, clinical-trial status changes, and adverse event dataset changes. It is data infrastructure only.

Request this feed View current demo Open paid API

GET /v1/regulatory/fda/changes?dataset=enforcement&product=medical-device&since=2026-07-01

{
  "data": [
    {
      "recordId": "sample-fda-2026-001",
      "dataset": "enforcement",
      "classification": "Class II",
      "productType": "medical-device",
      "reportedAt": "2026-07-02"
    }
  ],
  "meta": { "sampleOnly": true, "market": "fda-regulatory" }
}

Buyer Fit

This catalog entry summarizes the buyer fit, sources, and access model for this data product.

Recall and enforcement monitoring for operations workflows.
Dataset change feed for analysts and health-data applications.
Strictly public data, with no diagnosis, treatment, or safety advice.

Public Data Sources

The initial product would normalize public records into stable polling endpoints and exports.

openFDA public APIs
ClinicalTrials.gov public data API

Buyer Workflows

These are the specific self-serve workflows this page is designed to support.

Recall change monitoring

Poll public recall and enforcement datasets for new records that match a product category or company name.

Regulatory dataset deltas

Track public FDA dataset updates as normalized change records for research and compliance dashboards.

Trial-status watchlists

Monitor public clinical-trial records for status, sponsor, condition, or intervention changes.

Specific Workflow Tests

These pages focus on specific buyer workflows.

Workflow page FDA Recall API Public FDA recall and enforcement change monitoring Workflow page Clinical Trial Change API Clinical trial status and sponsor change monitoring Workflow page Clinical Trials API ClinicalTrials.gov API monitoring for trial status changes

Access Model

Pricing starts with narrow, low-touch access paths for qualified buyers.

Review the source coverage, sample response, and likely workflow fit.
Request access when the workflow matches a buyer use case.
Production availability depends on source scope, refresh cadence, and compliance boundaries.

Product FAQ

Is this a medical advice product?

No. The concept is public regulatory data infrastructure only and would avoid diagnosis, treatment, or safety guidance.

Why start with a focused public-data product?

The compliance risk and buyer specificity are higher, so the first release should stay narrow, source-linked, and reviewable before adding broader workflows.