About this source
Search the EMA’s EPAR list by name, active substance, therapeutic area or indication, and read the authorised indication, holder, ATC code, flags (orphan, biosimilar, conditional, PRIME) and every procedural date. Also EU orphan designations, direct healthcare professional communications and supply shortages. Refreshed twice a day; source acknowledged as EMA requires.
Questions you can ask EMA medicines
Type them into Kahubi’s chat once the source is connected.
“Find randomised trials of an intervention for a condition and list their identifiers.”
What comes back: Studies with registry or PubMed identifiers and key design details.
What the assistant can do with it
The 4 tools this server offers to Kahubi. The assistant picks the right one for each question.
ema_search_medicinesSearch EU centrally authorised medicines (EPARs, about 2,700).
ema_get_medicineFull EMA record for one medicine by name or EMEA/H/C product number: authorised therapeutic indication, INN, ATC, pharmacotherapeutic group, holder, every procedural date (opini...
ema_orphan_designationsEU orphan designations (about 3,300): active substance, intended rare-disease use, EU designation number, date, status (Positive, Withdrawn, Expired …) and the related authorise...
ema_safety_and_shortagesEMA safety communications to healthcare professionals (DHPCs: new risks, quality defects, restrictions) and medicine supply shortages, for a medicine, substance or therapeutic a...
Good to know
- Hosted by Kahubi. Kahubi runs this server itself so it stays reliable enough for research use.
- Cited, checkable answers. Results are treated as retrieved material and cited with the source’s own identifiers, so you can open every record the answer relied on.
- Your files stay private. Only the search the assistant writes for your question is sent to EMA medicines.
More medical & clinical sources
- PubMed & Europe PMCBiomedical literature: search, MeSH terms, related articles, citations and lawful full text.
- ClinicalTrials.govSearch registered clinical trials, read full study records, posted results and eligibility criteria.
- Clinical evidence (trials, FDA labels, adverse events)ClinicalTrials.gov, openFDA drug labels, adverse-event reports and approvals alongside PubMed.
- CDC data and WONDERUS public-health datasets (data.cdc.gov) and CDC WONDER mortality and natality queries.
- NCATS Inxight DrugsEvery FDA-registered substance with its UNII, plus NCATS-curated approval status, indications, targets and pharmacokinetics.
- openFDAFDA drug and device adverse events, recalls, labels and shortages.