News - Latest

1. New rules for the retail of veterinary medicines by online shops

   Commencing 28 January 2022, the date on which the new Veterinary Medicinal Products Regulation enters into force, the retail of ...

   News item | 20-01-2022 | 16:00

2. MEB fee rate change as of January 2022

   The Medicines Evaluation Board (MEB) increases the fee rates for authorisation applications, authorisation changes and the annual ...

   News item | 03-01-2022 | 10:00

3. Changes to policy on product information

   The Medicines Evaluation Board (MEB) has recently revised two policy documents for pharmaceutical companies in respect of the ...

   News item | 16-12-2021 | 10:00

4. New reporting process for the Medicine Shortages and Defects Notification Centre

   With effect from 1 January 2022, the Medicines Evaluation Board and the Health and Youth Care Inspectorate will be introducing ...

   News item | 01-12-2021 | 10:00

5. Veterinary Medicinal Products Regulation: QRD template, GMP certificates, OMS registration and EMA activities

   The entry into force of the Veterinary Medicinal Products Regulation ( Regulation (EU) 2019/6) on 28 January 2022 will result in ...

   News item | 24-11-2021 | 12:00

6. Newest issue of Regulatory Science Magazine

   Today we have published the latest edition of our online science magazine: Regulatory Science Magazine. This edition contains the ...

   News item | 12-10-2021 | 11:00

7. Veterinary Medicinal Products Regulation: link between EudraGMDP database and OMS

   A number of things are going to change in relation to the EudraGMDP database in the field of veterinary medicinal products. This ...

   News item | 07-10-2021 | 17:00

8. Veterinary Medicinal Products Unit Fees for 2022

   A lot of procedures are going to change as a consequence of the Veterinary Medicinal Products Regulation ( Regulation (EU) ...

   News item | 04-10-2021 | 12:30

9. Medicine shortages and defects notification centre form improved

   The notification form of the Medicine Shortages and Defects Notification Centre has been made more user-friendly. Various ...

   News item | 01-10-2021 | 13:00

10. Veterinary pharmacovigilance: important change relating to the submission of reports of adverse events

    As a marketing authorisation holder you are obliged to submit reports of adverse events to the medicinal product authorities. ...

    News item | 30-09-2021 | 10:00