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Stricter requirements on the packaging of medicinal products to prevent falsification

The packaging of certain medicinal products for human use must have safety features implemented before 9 February 2019. This is ...

News item | 15-12-2016 | 16:30

Bert Leufkens stepping down as MEB chairman

The chairman of the Medicines Evaluation Board (MEB), Bert Leufkens, today announced that he is stepping down as chair as of 1 ...

News item | 01-12-2016 | 12:30

MEB joins European partnership on research into Alzheimer's disease

The Medicines Evaluation Board (MEB), in cooperation with another 22 organisations in 6 countries, is participating in a European ...

News item | 29-11-2016 | 17:00

The MEB does not accept gifts

Towards the end of the year, the MEB is offered gifts by some organisations. In order to maintain independence and impartiality, ...

News item | 23-11-2016 | 16:00

Additional instructions for in-use shelf life OTC medicinal products

The Medicines Evaluation Board (MEB) is requesting manufacturers of multidose medicinal products that do not require a ...

News item | 23-11-2016 | 11:30

Public consultation on assessment criteria for combination packages policy

The Medicines Evaluation Board (MEB) invites interested parties and stakeholders to comment on the draft policy document on the ...

News item | 17-11-2016 | 16:00

In-use shelf life to be listed on packaging of over-the-counter medicinal products

The Medicines Evaluation Board (MEB) wants manufacturers of over-the-counter medicinal products to list the in-use shelf life on ...

News item | 30-09-2016 | 10:30

Henk-Jan Guchelaar sworn in as new MEB member

Prof. H.J. (Henk-Jan) Guchelaar was sworn in as new member of the Medicines Evaluation Board (MEB) today. He was appointed as of ...

News item | 25-08-2016 | 16:00

Guidance on the Substantiation of Claims made on Animal Nutrition updated

The Guidance on the Substantiation of Claims made on Animal Nutrition has been updated as of 18 August 2016.

News item | 18-08-2016 | 12:00

Start of European registration of PSURs

All PSURS for centrally and nationally authorised medicinal products in Europe must be submitted via the PSUR Repository as of 13 ...

News item | 08-07-2016 | 15:00