The EMA relocation is a direct consequence of the United Kingdom’s decision to leave the European Union. EMA has been based in London, UK, since it was established in 1995 and currently employs around 900 staff members at its headquarters in Canary Wharf, London. A total of nineteen cities from across the EU made bids to host the agency, with Amsterdam coming out on top. EMA Executive Director Guido Rasi stated, “My staff and I are very honored that so many Member States showed an interest in hosting EMA.”
Dutch Minister of Foreign Affairs Halbe Zijlstra was very positive about the result: ‘This is a fantastic outcome. It’s good for the Netherlands, but above all, it’s good for EU citizens who can continue to count on high-quality medicines and proper supervision of medicines. It shows that we can tackle the effects of Brexit with resolve.”
Professor Rasi was happy with the Amsterdam decision: “Amsterdam ticks many of our boxes. It offers excellent connectivity and a building that can be shaped according to our needs. I am very grateful that the Member States took into account our requirements for business continuity and gave priority to the protection of public and animal health.”
Efficacy, quality and safety
EMA is the body responsible for assessing the efficacy, quality, and safety of new medicines, for human and animal health, before they are approved for the European market. In addition, the organization supervises the safety of authorized medicines and promotes research into and the development of new medicines. Every year EMA organizes hundreds of meetings for thousands of experts from Europe and further afield.
The organization has approximately 900 highly qualified staff from all the EU member states. A large majority of EMA staff expressed their willingness to move with the agency to the new home in Amsterdam. The EU had set out six criteria to be met when evaluating candidate locations, including the city’s ability to get the agency fully operational on time, transport accessibility, available schooling, and employment opportunities for spouses.
European pharmaceutical network
The Dutch Medicines Evaluation Board (CBG) is a major contributor of expertise to the European network of pharmaceutical authorities coordinated by EMA. A large number of pharmaceutical organizations are currently located in London, many of whom work intensively with EMA. It is likely that at least some of these organizations will want to relocate to the same place as EMA. This could potentially strengthen the Dutch position in European pharmaceutical policy and boost the Netherlands’ attractiveness to companies and institutions in the top sectors of life sciences and health, and agrifood.
Dutch Minister for Healthcare, Bruno Bruins commented: ‘This is good news for all patients across Europe. In Amsterdam, the EMA will be able to continue its important work without interruption after Brexit. The Agency can continue to grant access to new, innovative medicines without delay.” He added: “Now, the real work begins. Amsterdam and the Netherlands as a whole are fully committed to ensuring the EMA’s relocation runs smoothly. We are ready to get started and we will make sure that the EMA’s important work is not disrupted.”
Effective collaboration between EMA and the Netherlands on the basis of the commitments made in its offer to host EMA is the key to ensuring a successful move and the continuation of EMA’s operations with minimal disruption. The Agency now has just over 16 months to prepare for the move and take up its operations in Amsterdam on 30 March 2019 at the latest.
Source / Investinholland.com