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May 1, 2012 - Productive workshop about reducing the use of laboratory animals

For many years now, the aim has been to use mouse embryonic stem cells for research into the safety of substances during pregnancy. To this end, a workshop was held in Leiden in which employees from American and European authorities and experts from the medicines industry and universities participated.

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April 27, 2012 - Informative meeting new pharmacovigilance legislation on 24 April 2012

On 24 april 2012 the Medicines Evaluation Board (MEB) organised another informative meeting in Utrecht about the implications of the new pharmacovigilance legislation. This meeting with 200 participants was primarily targeted at marketing authorisation holders.

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April 25, 2012 - Presentation about Common European Submission Platform

On 19 April 2012, Stan van Belkum – employee at the Medicines Evaluation Board (MEB) – gave a presentation about CESP for Regned.

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April 17, 2012 - CHMP bids farewell to its chairman with a standing ovation

The CHMP, the scientific committee of the European Medicines Agency (EMA), in which the Medicines Evaluation Board (MEB) is represented, said goodbye to its chairman Dr Eric Abadie with great appreciation in London on 16 April 2012.

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April 13, 2012 - Results of the CORE study

The CORE study is a PhD research project carried out within the Department of Clinical Pharmacology at the University Medical Center Groningen (UMCG), in collaboration with the Medicines Evaluation Board (MEB).

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March 28, 2012 - Look back at the Dies lecture Utrecht University

On Monday 26 March 2012, the University of Utrecht celebrated its 376th birthday – the Dies Natalis – in the Dom church. There was great interest in this traditional gathering centred on the theme of ‘Life Sciences’.

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March 26, 2012 - MEB chairman gives Dies lecture University Utrecht

Today – on 26 March 2012, the 376th Dies Natalis of the University of Utrecht will take place. The theme for this year is Life Sciences, one of the strategic goals of the university. MEB chairman and professor of Pharmacoepidemiology, Prof Bert Leufkens, is extremely honoured to give the Dies lecture.

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March 9, 2012 - Clinical practice central to the quarterly consultation between MEB and patient and consumer organisations

The quarterly consultation between the Medicines Evaluation Board (MEB) and patient and consumer organisations took place on Wednesday 7 March 2012. The discussion during the consultation focused on clinical practice: what are the problems that patients experience in using their medicines?

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February 29, 2012 - MEB has moved to Utrecht - new address as of 29 February 2012

The Medicines Evaluation Board (MEB) has moved to Utrecht. As of 29 February 2012 we have a new address.

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February 15, 2012 - Public MEB reports partially updated

The Medicines Evaluation Board (MEB) has updated the public reports for MEB Meetings 721 to 730.

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February 3, 2012 - MEB signs new code to prevent being influenced by a conflict of interests

The Medicines Evaluation Board (MEB) has signed a Code together with more than thirty organisations in order to prevent a possible conflict of interests. For example, the interests of experts who form part of scientific and advice committees are disclosed via the code in order to prevent a conflict of interests and thereby improper influences.

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January 19, 2012 - The MEB is moving to Utrecht this year

The MEB, which currently has 6 offices throughout the country, moves to one central location in Utrecht on 29 February 2012. The MEB remains connected to the University Medical Centre Groningen and the University Medical Centre St. Radboud in Nijmegen. These two institutions can be reached via the general telephone number and postal address.

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January 5, 2012 - Common European Submission Platform: Extended Proof of Concept

Under the remit of the Heads of Medicines Agency (HMA), a group of Agencies and Industry Representatives have been working to investigate the feasibility for the development of a Common European Submission Platform (CESP). A Proof of Concept was run during September and October 2011 and following its success the next steps for CESP were agreed at the Heads of Medicines Agency (HMA) meeting in November 2011.

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