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Empty SPC template – QRD 8.2 (centralised)

Form | 07-01-2021

Product types and fees, veterinary

Publication | 26-11-2020

GS-list 18

The list of active substances in products that may qualify for sale general sale (GS list) was updated by the MEB on 22 October ...

Policy document | 22-10-2020

Terms and conditions for package fee and reduced fee for copy DCP application - human products

The term package fee entails that a group of products (each with an individual RVG number) is only billed once at the tariff ...

Publication | 01-09-2020

Summary - Report on paracetamol and PCA

Report | 27-08-2020

Report on paracetamol and PCA

Report | 26-08-2020

MEB 43: Two-round assessment policy for national procedures

Limiting the number of assessment rounds ensures that the (legally) stipulated time within which the MEB must make a decision ...

Policy document | 01-08-2020

Withdrawal of marketing authorisation at the request of the marketing authorisation holder

A marketing authorisation holder may decide to have their marketing authorisation withdrawn for various reasons. After completing ...

Form | 01-08-2020

MEB 14: Parallel importation: marketing authorisation and maintenance

Parallel import is the importation – and subsequent marketing in the Netherlands – of a medicinal product authorised elsewhere in ...

Policy document | 27-05-2020

Strategic Business Plan 2020-2024

This Strategic Business Plan (SBP) describes the strategic direction of the Medicines Evaluation Board (MEB) in the coming period ...

Publication | 21-04-2020