Overview regulatory data

Show available data sets publicly provided by medicine regulatory agencies
data
Author

Ralf Herold

Published

2026-10-18

Modified

2026-10-18

Overview

This page provides an overview to the data sets and information made publicly availalbe by medicine regulatory agencies. At this time, it includes references to only the EMA. The webapp below is for finding data related to

  • documents

  • DHPCs (dear health care professional communications)

  • medicine shortages in the EU

  • scientific guidelines

  • medicines used outside the EU

  • periodic safety update single assessments

  • post-authorisation referrals

  • orphan designations

  • paediatric investigation plans

The content of source(s) of data of interest can be accessed here as follows.

Source at EMA Type of data This site provides Access here to
Novel methodologies Link PDF files (Submission, letter of support, opinion) Webapp Structured project information1
Paediatric investigation plans (including waivers) Link PDF files (Decisions, Opinions) Webapp2 PDF files content (English only) searchable and structured
Orphan designation Link PDF files (Summary of opinion), structured product webpage None None
Clinical trials Link Structured webpage, PDF files (i.a., protocol, reports, SIS, ICF) R package Content via scripting
Medicine assessments (Human use, centrally authorised) Link PDF files (assessment reports, variation reports, risk management system), structured product webpage Webapp PDF files content (English only) searchable and structured
Clinical data publication3 Link PDF files (Clinical study reports, CSRs, Overviews, Summaries, Anonymisation reports) None Under consideration

1 Includes Drug Development Tool (DDT) Qualification Programs by the FDA, see here.

2 Includes historical versions and modifications

3 For clinical data provided by Health Canada, see here.

Webapp of data references

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