# EUR-Lex Pharma

This provider exposes tools and data accessible through its parent verticals. Use the example prompts as inspiration for your queries.

**Slug:** `eurlex`

**Description:** Search and inspect EU Commission Decisions on centralised marketing authorisations for medicinal products — the legal acts underlying every EMA EPAR (granting, varying, suspending, or withdrawing an authorisation under Regulation (EC) No 726/2004). Data sourced from EUR-Lex monthly OJ C-series summaries via the Publications Office Cellar SPARQL endpoint.

## Verticals

This provider is available in the following verticals:

- [Medical](https://kirha.com/verticals/medical.md)

## Example prompts (non-exhaustive)

- `When was REZUROCK first authorised in the EU?`
- `All Commission decisions for OPDIVO`
- `Recent EU MA decisions involving Sanofi`
- `Timeline of authorisation EU/1/26/2015`
- `EU MA withdrawals in the last 12 months`
- `All centralised authorisations containing semaglutide`
- `What's in summary 52026XC02325?`

## Available tools in this provider

Open a tool to see its input and output schemas.

### [`listRecentWithdrawalsAndSuspensions`](https://kirha.com/providers/eurlex/listRecentWithdrawalsAndSuspensions.md)

List the most recent EU Commission decisions that withdraw or suspend centralised marketing authorisations. Pharmacovigilance / market-access view of high-signal regulatory events. Optionally scope to a single holder.

### [`searchDecisionsByRegisterNumber`](https://kirha.com/providers/eurlex/searchDecisionsByRegisterNumber.md)

Find every EU Commission Decision (initial grant + variations + withdrawals + suspensions) tied to a given EU Community Register number (EU/1/YY/NNNN), returned in chronological order. This is the canonical per-product identifier used by EUR-Lex summary documents. NOTE: the EMA EPAR number `EMEA/H/C/NNNNNN` is a different identifier and will NOT match here — to bridge from EMA data, search by product name first.

### [`searchDecisionsByProduct`](https://kirha.com/providers/eurlex/searchDecisionsByProduct.md)

Full-text search across EU Commission Decisions on centralised marketing authorisations by medicinal product name. Returns each decision row (issuing / modification / withdrawal / suspension / rejection) with its date, EU register number, holder, pharmaceutical form, ATC code, and a link to the parent monthly summary in EUR-Lex. Use this as the entry point when the user mentions a product name. Returns euRegisterNumbers and summaryCelexes for composition with other tools.

### [`searchDecisionsByINN`](https://kirha.com/providers/eurlex/searchDecisionsByINN.md)

Find EU Commission Decisions for products containing a given active substance (INN — international non-proprietary name). Returns both branded and biosimilar/generic centralised authorisations. NOTE: only 'issuing' (initial grant) decisions carry an INN field in the source data — modification, withdrawal and suspension rows do not. To track the full lifecycle of an INN, follow up with searchDecisionsByRegisterNumber on each EU register number returned.

### [`searchDecisionsByHolder`](https://kirha.com/providers/eurlex/searchDecisionsByHolder.md)

Find EU Commission Decisions involving a given marketing authorisation holder (laboratoire titulaire — e.g. 'Roche Registration GmbH', 'Novartis Europharm Limited'). Use to answer 'recent decisions for Sanofi' or to enumerate a company's EU centralised authorisation activity.

### [`searchDecisionsByDateRange`](https://kirha.com/providers/eurlex/searchDecisionsByDateRange.md)

List EU Commission Decisions on centralised marketing authorisations within a date range, optionally narrowed to a specific decision type. Use for regulatory-news monitoring ('what was authorised last quarter?') or compliance reporting.

### [`getMonthlySummary`](https://kirha.com/providers/eurlex/getMonthlySummary.md)

Return the full monthly OJ C-series summary document by its CELEX (e.g. '52026XC02325') — publication date, title, URL, and every decision row inside it grouped by section (issuing / modification / withdrawal / suspension / rejection). Use this when an agent has a summary CELEX from a prior search and wants the full source document.

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**Tags:** pharma, regulatory, eu, eur-lex, medicines, legal

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