Welcome to Rhizome API
The Rhizome API provides programmatic access to search and retrieve regulatory documents from the FDA, EMA, and other regulatory agencies.Search Documents
Search across regulatory documents with keyword matching and get page-level
results.
Get Document Contents
Retrieve the full text of any document page by page.
Quick Start
1. Get your API Key
Visit the API Keys console to create an API key.2. Make your first request
3. Explore the results
The search returns page-level results with the matched text:4. Get full document
Use thedoc_id to retrieve all pages:
Available Datasets
FDA Datasets
| Dataset | Description |
|---|---|
fda_drug | FDA drug approval documents (NDAs, ANDAs) |
fda_biologic | FDA biologic license applications (BLAs) |
fda_denovo_or_510k | FDA 510(k) and De Novo device clearances |
fda_pma | FDA PMA device approvals |
fda_guidance | FDA guidance documents |
fda_warning_letters | FDA warning letters to companies |
fda_clinical_trials | Clinical trial data from ClinicalTrials.gov |
fda_483 | FDA 483 inspection observations |
fda_inspections | FDA inspection records |
fda_recalls | FDA recall notices |
fda_crl | FDA Complete Response Letters |
fda_ufa | FDA User Fee Act reports |
fda_recall_enforcement | FDA recall enforcement reports |
fda_maude | FDA MAUDE adverse event reports |
fda_faers | FDA FAERS adverse event reports |
EMA Datasets
| Dataset | Description |
|---|---|
ema_epar | EMA European Public Assessment Reports |
ema_guidelines | EMA guidance documents |
ema_ctis | EMA Clinical Trials Information System |
ema_pip | EMA Paediatric Investigation Plans |
ema_committee | EMA committee meeting documents |
ema_mdcg_guidance | Medical Device Coordination Group guidance |
Other Regulatory Agencies
| Dataset | Description |
|---|---|
canada_guidance | Health Canada guidance documents |
canada_par | Health Canada Public Assessment Reports |
canada_clinical_trials | Health Canada clinical trials |
swiss_par | Swissmedic Public Assessment Reports |
swiss_guidance | Swissmedic guidance documents |
swiss_clinical_trials | Swiss clinical trials |
mhra_ct | MHRA clinical trials |
mhra_pr | MHRA public assessment reports |
mhra_guidance | MHRA guidance documents |
tga_guidance | TGA (Australia) guidance documents |
eu_ctr | EU Clinical Trials Register |
ich_guidelines | ICH harmonized guidelines |