EU Health & Compliance Data API
Pricing
$3.00 / 1,000 data records
EU Health & Compliance Data API
Search EU medicines, medical devices, clinical trials, food safety, environmental, and health datasets in one run. Get structured records fast.
Pricing
$3.00 / 1,000 data records
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0.0
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Developer
kane liu
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1
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1
Monthly active users
11 days ago
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EU Health & Compliance Data Search
Search 17 EU health and compliance data sources in one query — EMA medicines, EUDAMED medical devices, CTIS clinical trials, ECDC surveillance, EFSA toxicology, EU Ecolabel, EMAS registrations, and E-PRTR emissions.
- ✅ Search 17 EU health and compliance data sources across medicines, devices, clinical surveillance, and environmental or regulatory records
- ✅ Get authorized medicines, EPAR documents, orphan designations, medical devices, clinical trials, disease surveillance, food toxicology, and environmental compliance data in one workflow
- ✅ Covers 9 EMA medicines sources, 1 medical device source, 2 clinical and surveillance sources, and 5 environmental or compliance sources
- ✅ Export results as Excel, CSV, or JSON, or connect it to Apify MCP, API, Make, n8n, and Zapier
- ✅ Current Apify listing is pay per usage, so you can start with small runs and scale only when the workflow proves useful
EU health and compliance data is spread across EMA, EUDAMED, CTIS, ECDC, EFSA, EU Ecolabel, EMAS, E-PRTR, and other European-level public systems. If you want to check a medicine, device, trial, disease topic, or compliance record, the usual workflow means searching multiple regulators one by one. This Actor turns that process into one searchable dataset you can export or automate.
What you can do with it
1. Search EMA authorized medicines, safety records, and regulatory documents in one run
When you look up a medicine in the EU, you often need more than one EMA source. A product may appear in the authorized medicines database, EPAR assessment documents, herbal medicines, orphan designations, paediatric plans, post-authorisation records, shortages, PSUSAs, or safety communications. This Actor lets you search that active EMA set together.
To run this, all you fill in are a search term, the EMA medicines category toggle, and how many results you want per source.
What you enter:
| What | Example |
|---|---|
| Search term | ibuprofen |
| Categories | EMA medicines only |
| How many results | 50 per source |
Click Start. The Actor queries the active EMA sources and returns matching records:
What you get back:
| Source | Example fields |
|---|---|
| EMA medicines | Medicine name, active substance, authorisation status, holder, therapeutic area |
| EPAR documents | Product name, document title, document type, publication metadata |
| Orphan designations | Medicine name, condition, sponsor, designation number, status |
| Shortages and safety | Product name, shortage or safety status, dates, communications metadata |
This is useful for regulatory research, pharmacovigilance support, drug-market monitoring, and AI workflows where one medicine term needs to fan out across multiple EMA public datasets.
2. Search EUDAMED medical devices across the EU device registry
Medical-device workflows often start with one core question: does this product, manufacturer, or device family appear in EUDAMED? This Actor includes the active EUDAMED medical devices source, which is currently the dedicated device component of the search flow.
That makes it useful when you want to search EU medical-device records without opening the device database separately from the rest of the EU health stack.
What you enter:
| What | Example |
|---|---|
| Search term | pacemaker, cardiac, stent, or a manufacturer name |
| Categories | Medical devices only |
| How many results | 50 |
What you get back:
| Source | Example fields |
|---|---|
| EUDAMED medical devices | Device name, manufacturer, risk class, UDI-related data, device status |
This is a practical starting point for device-market research, regulatory screening, procurement support, and product discovery workflows where device results need to be combined with medicine, trial, or surveillance results.
3. Search CTIS clinical trials and ECDC surveillance together
Clinical and disease-monitoring workflows often need more than one public source. A therapeutic area may appear in CTIS trial records and also in ECDC surveillance datasets. This Actor lets you search those active public clinical and surveillance sources together.
That means one query can return trial records and surveillance-oriented records in the same run.
What you enter:
| What | Example |
|---|---|
| Search term | influenza, diabetes, covid, oncology |
| Categories | Clinical trials and surveillance |
| How many results | 50 per source |
What you get back:
| Source | Example fields |
|---|---|
| CTIS clinical trials | Trial title, sponsor, recruitment status, condition, member-state context |
| ECDC surveillance | Disease or surveillance record, country or member state, reporting metadata |
This is useful for clinical-intelligence workflows, epidemiology support, public-health monitoring, and AI research systems that need one search layer across trials and surveillance.
4. Review food toxicology, ecolabel, environmental management, emissions, and sanctions records
The environmental and compliance group brings together five different EU public sources:
EU EcolabelproductsEFSA OpenFoodToxEMASregistrationsE-PRTRindustrial emissionsESMAsanctions
These are not the same kind of record, and that is exactly why combining them is useful. One workflow may need product labels, toxicology references, environmental registrations, emissions data, or sanctions-related records, depending on the entity or topic you are checking.
What you enter:
| What | Example |
|---|---|
| Search term | glyphosate, detergent, emissions, market abuse |
| Categories | Environmental and compliance only |
| How many results | 50 per source |
What you get back:
| Source | Example fields |
|---|---|
| EFSA OpenFoodTox | Substance name, toxicology record type, status or hazard-related metadata |
| EU Ecolabel | Product name, license holder, product group, country |
| EMAS registrations | Organisation name, registration status, country |
| E-PRTR emissions | Facility or operator, country, pollutant or emissions context |
| ESMA sanctions | Entity name, sanction record, authority or jurisdiction context |
This is useful for product-compliance research, environmental monitoring, sanctions and enforcement review, and cross-regulator due diligence across EU public sources.
5. Use it from ChatGPT, Claude, or no-code automation
This Actor also works as an EU health and compliance search layer inside AI assistants and automation systems. Instead of teaching each workflow how to query EMA, EUDAMED, CTIS, ECDC, EFSA, EMAS, and E-PRTR separately, you can use one Actor as the search layer.
Connect it once through Apify MCP, API, or a no-code platform, then ask for the results you need:
What you enter:
| What | Example |
|---|---|
| Search term | ibuprofen |
| Categories | EMA medicines + clinical trials |
| Result limit | 25 |
What your assistant or automation gets back:
| Source | Returned data |
|---|---|
| EMA | Medicines, EPAR, safety, shortages, and related records |
| CTIS and ECDC | Trial and surveillance results |
| Other EU compliance sources | Included if those category toggles are enabled |
That makes it useful for internal AI research assistants, regulatory monitoring, pharmacovigilance support, and spreadsheet-based search workflows that need one EU public-data entry point.
How to use (no code required)
- Click "Try for Free" at the top of this page
- Type one or more search terms — medicine names, device types, diseases, substances, organisations, or regulatory keywords
- Choose which categories to search:
- EMA medicines and drug safety
- medical devices
- clinical trials and surveillance
- environmental and compliance
- Set how many results you want per source
- Click Start — the Actor queries the enabled EU public data sources and returns the results in the Dataset tab
You can then export the results as Excel, CSV, or JSON.
This Actor uses the SIP Public Data Gateway and queries the active EU health and compliance source set over HTTP. No browser setup, no regulator-by-regulator integration work, and no need to open each system manually.
Because the Actor is listed as pay per usage, it is straightforward to start with a small exploratory run, validate that the source mix is useful, and then expand the workflow.
What you get back
Each result comes back as one row in a dataset. The exact columns vary by source family, because an EMA medicine record, a CTIS trial, a device entry, and an emissions record do not share the same schema.
Across the dataset, you will typically see:
nametypestatuscountryauthority_product_id_source_search_term_collected_at
Then source-specific fields such as:
- EMA: medicine name, active substance, authorisation status, sponsor, document or designation fields
- Medical devices: device name, manufacturer, risk class, UDI-related fields
- Clinical and surveillance: trial title, sponsor, condition, reporting country, surveillance metadata
- Environmental and compliance: organisation or facility name, pollutant, toxicology record, registration status, sanction or ecolabel fields
Every row tells you which source it came from and which search term matched. That makes it easy to filter by source family, split exports by authority, or merge the results into downstream workflows.
Coverage
This Actor currently searches 17 active EU health and compliance data sources:
| Category | Count | Coverage |
|---|---|---|
| EMA medicines | 9 | Authorized medicines, EPAR documents, herbal medicines, orphan designations, paediatric plans, post-authorisation records, shortages, PSUSAs, safety communications |
| Medical devices | 1 | EUDAMED medical devices |
| Clinical and surveillance | 2 | CTIS clinical trials and ECDC surveillance |
| Environmental and compliance | 5 | EU Ecolabel, EFSA OpenFoodTox, EMAS registrations, E-PRTR industrial emissions, ESMA sanctions |
The current active maps in the Actor are:
9 EMA medicines sources1 medical device source2 clinical and surveillance sources5 environmental and compliance sources
That mix matters, because this Actor is not just one EU register. It is a combined EU health and compliance search layer across several different European public systems.
Pricing
This Actor is currently listed on Apify as pay per usage.
The safest place to check the current commercial terms is the live pricing tab:
If you want to control spend, the easiest approach is to:
- search only the categories you need
- start with one or two search terms
- lower
maxResultsPerSourcefor exploratory runs
Connect to your tools
You can use this Actor directly in the Apify UI, or connect it to automation and AI workflows:
| Platform | How to connect |
|---|---|
| Apify UI | Run it directly and export results |
| Apify API | Trigger runs and fetch datasets programmatically |
| Make.com | Use the Actor ID lentic_clockss/eu-health-compliance-search |
| n8n / Zapier / ChatGPT / Claude | Use the same Actor ID via Apify MCP or API |
Related Actors
- EU Business Data Search — EU business and registry sources
- EU Financial Data Search — ECB, EBA, and financial registers
- UK Data Search — UK public data across multiple source families
- Taiwan Data Search — Taiwan health, compliance, market, and environment sources
→ Browse all Actors: apify.com/lentic_clockss
Also Available
- Direct API:
https://opendata.best/api/v1/data - Postman Collection: Fork and test
- GitHub: Collection source files