Integration of EudraGMDP and OMS - Webinar for industry
The new regulatory framework for veterinary medicines requires several changes to EudraGMDP. The most notable change is the integration of EudraGMDP with EMA’s Organisation Management Service (OMS).
From 28 January 2022, users of EudraGMDP from national competent authorities will no longer introduce organisational data (organisation name and location address details) directly into the relevant fields on the EudraGMDP database. Instead, they will select the relevant organisation name and location address details, including the legally registered address, of the manufacturers/importers/distributors from the Agency’s organisation dictionary (so-called OMS).
It is therefore necessary that as of 28 January 2022, before applying for a new/updated manufacturing or wholesale distribution authorisation with national competent authorities, organisations verify that their relevant locations are correctly recorded in OMS. This applies to all organisations which appear on documents within EudraGMDP, including EU and non-EU manufacturers, importers and distributors of human and veterinary medicinal products and active substances.
The webinar for industry users covers:
- Integration of EudraGMDP and OMS – implications for industry users;
- OMS services and activities;
- OMS change request process;
- customer service (EMA Service Desk)
- data quality management.
Questions and answers from the webinar for industry on integration of EudraGMDP and OMS (PDF/173.58 KB)
First published: 16/11/2021
Presentation: Industry webinar - Introduction to Organisation Management Services (OMS) and activities (PDF/2.01 MB)
First published: 21/10/2021
Presentation - Integration of EudraGMDP and OMS: implications for industry users (M. Filancia, EMA) (PDF/2.43 MB)
First published: 26/10/2021