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Pharma

Mapping marketing authorisations across 36 countries

Sales teams have a single workbook of authorised products containing their molecules, country by country, with the manufacturing sites. Every data point links to the official page and the text extract that supports it.

Illustrative mock-up of the tool : authorisations · workbook by country
Illustrative mock-up: the names, values and documents shown are fictitious.

Context

A pharmaceutical group that manufactures active ingredients wants to know where its molecules are marketed and who manufactures the finished products.

The problem

The information exists but is scattered across 36 national regulatory registers, in as many languages and formats, with no common interface.

What we built

An agentic collection and qualification pipeline: identification of each country's official register, extraction of 25 fields per product, reading of package leaflets and summaries of product characteristics to find the manufacturing sites, automatic checks (direct links to the product record, no generic search page, unique identifiers) and traceability of every value back to its source URL with the extract that proves it.

Steps

  1. 01Locating and testing each country's official register (EU, United Kingdom, United States, Canada, Brazil, Japan, Australia)
  2. 02Product-by-product extraction, by substance name and brand names
  3. 03Reading regulatory documents for manufacturing sites, with a cited extract
  4. 04Controlled propagation between European countries for mutual recognition procedures
  5. 05Automatic quality control, then a findings report and workbook

Hosting and models

Not documented in the files opened (the report describes the sources and pipelines, not the models or hosting).

Services involved

Forward Deployed Engineers · Agentic platforms

We name a client only with their written agreement. The budgets and detailed results of our engagements remain confidential.

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