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EU Health & Compliance Data API

Pricing

$3.00 / 1,000 data records

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EU Health & Compliance Data API

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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kane liu

kane liu

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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:

WhatExample
Search termibuprofen
CategoriesEMA medicines only
How many results50 per source

Click Start. The Actor queries the active EMA sources and returns matching records:

What you get back:

SourceExample fields
EMA medicinesMedicine name, active substance, authorisation status, holder, therapeutic area
EPAR documentsProduct name, document title, document type, publication metadata
Orphan designationsMedicine name, condition, sponsor, designation number, status
Shortages and safetyProduct 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:

WhatExample
Search termpacemaker, cardiac, stent, or a manufacturer name
CategoriesMedical devices only
How many results50

What you get back:

SourceExample fields
EUDAMED medical devicesDevice 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:

WhatExample
Search terminfluenza, diabetes, covid, oncology
CategoriesClinical trials and surveillance
How many results50 per source

What you get back:

SourceExample fields
CTIS clinical trialsTrial title, sponsor, recruitment status, condition, member-state context
ECDC surveillanceDisease 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 Ecolabel products
  • EFSA OpenFoodTox
  • EMAS registrations
  • E-PRTR industrial emissions
  • ESMA sanctions

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:

WhatExample
Search termglyphosate, detergent, emissions, market abuse
CategoriesEnvironmental and compliance only
How many results50 per source

What you get back:

SourceExample fields
EFSA OpenFoodToxSubstance name, toxicology record type, status or hazard-related metadata
EU EcolabelProduct name, license holder, product group, country
EMAS registrationsOrganisation name, registration status, country
E-PRTR emissionsFacility or operator, country, pollutant or emissions context
ESMA sanctionsEntity 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:

WhatExample
Search termibuprofen
CategoriesEMA medicines + clinical trials
Result limit25

What your assistant or automation gets back:

SourceReturned data
EMAMedicines, EPAR, safety, shortages, and related records
CTIS and ECDCTrial and surveillance results
Other EU compliance sourcesIncluded 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)

  1. Click "Try for Free" at the top of this page
  2. Type one or more search terms — medicine names, device types, diseases, substances, organisations, or regulatory keywords
  3. Choose which categories to search:
    • EMA medicines and drug safety
    • medical devices
    • clinical trials and surveillance
    • environmental and compliance
  4. Set how many results you want per source
  5. 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:

  • name
  • type
  • status
  • country
  • authority
  • _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:

CategoryCountCoverage
EMA medicines9Authorized medicines, EPAR documents, herbal medicines, orphan designations, paediatric plans, post-authorisation records, shortages, PSUSAs, safety communications
Medical devices1EUDAMED medical devices
Clinical and surveillance2CTIS clinical trials and ECDC surveillance
Environmental and compliance5EU Ecolabel, EFSA OpenFoodTox, EMAS registrations, E-PRTR industrial emissions, ESMA sanctions

The current active maps in the Actor are:

  • 9 EMA medicines sources
  • 1 medical device source
  • 2 clinical and surveillance sources
  • 5 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 maxResultsPerSource for exploratory runs

Connect to your tools

You can use this Actor directly in the Apify UI, or connect it to automation and AI workflows:

PlatformHow to connect
Apify UIRun it directly and export results
Apify APITrigger runs and fetch datasets programmatically
Make.comUse the Actor ID lentic_clockss/eu-health-compliance-search
n8n / Zapier / ChatGPT / ClaudeUse the same Actor ID via Apify MCP or API

→ Browse all Actors: apify.com/lentic_clockss


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