Welcome to MedDRA

In the late 1990s, the International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) developed MedDRA, a rich and highly specific standardised medical terminology to facilitate sharing of regulatory information internationally for medical products used by humans... (more)

Discover MedDRA

"Understanding MedDRA"

Learn more about MedDRA

MedDRA Training

Improve your skills

MVAT

Impact of MedDRA versions on your data

Support Documentation

MedDRA Points to Consider

Analysis Tool

Standardised MedDRA Queries (SMQs)

MedDRA Access

How to subscribe

MedDRA Training

15 January 2015
Bagsvaerd, Denmark
16 January 2015
Bagsværd, Denmark
28 January 2015
Paris, France
3 February 2015
London, United Kingdom

Help to Shape the MedDRA Terminology

by submitting change requests. Your contribution will then be considered by the MSSO/JMO.

WebCR

Recent News

21 November 2014

The 2015 MedDRA training schedule has been posted

18 November 2014

ICH MedDRA Management Board Endorses Blue Ribbon Panel Recommendations for a 27th SOC

17 November 2014

Date: 3 December at 15:00 CET / 9:00 EST.  Topic:  MedDRA Coding and Retrieval Conventions, Related SOPs, and Controlled Documents