Medicines and Healthcare Products Regulatory Agency information day: Medical Dictionary for Regulatory Activities in the pharmacovigilance regulatory process

• Date:
  Monday, 8 December 2014, All day
• Location:
  European Medicines Agency, Amsterdam, the Netherlands

This information day will provide attendees with a highlight of the latest Medical Dictionary for Regulatory Activities (MedDRA) initiatives and developments. This will includes an outline of various efforts of the MedDRA Maintenance and Support Services Organization (MSSO) to supportinteroperability of MedDRA with other terminologies specifically in the healthcare domain and the useof MedDRA in coding and analysing medication errors. Places limited.

Documents

Agenda and registration form - Medicines and Healthcare Products Regulatory Agency information day: Medical Dictionary for Regulatory Activities in the pharmacovigilance regulatory process

Summary:

The Medical Dictionary for Regulatory Activities (MedDRA) terminology is designed to assist the

sharing, assessment and evaluation of medical information in relation to the authorisation, the safety

monitoring and continuous benefit risk assessment of medicines.