EMA prepares to scale back more activities ahead of move

"Staff who will not relocate to Amsterdam have already started to leave the Agency," the EMA said in a statement, "and this trend is expected to accelerate. In addition, due to the employment rules in the Netherlands, 135 short-term contract staff will no longer be able to work for EMA.

"Overall, EMA expects a staff loss of about 30%, with a high degree of uncertainty regarding mid-term staff retention."

The Agency added that it has put in place supporting measures to facilitate the relocation of staff to Amsterdam and additional support is provided by the Dutch government. Other mitigating actions, such as a comprehensive staff recruitment programme, are already underway. However, in the short- to mid-term EMA will have to reprioritise its resources to fully maintain its core activities related to the evaluation and supervision of medicines to the level of quality and within the timelines expected.

The next phase of the continuity plan therefore involves scaling back or suspending additional activities through to 2018.

These activities include:

Collaboration at international level, which will be temporarily scaled back to focus primarily on product-related requests, supply-chain integrity and procedures under Article 58; in other areas, such as the harmonisation of global medicine regulation, EMA will only take a reactive role; EMA’s engagement in other global public health issues such as antimicrobial resistance or vaccines will be maintained as long as possible, but reviewed on a case-by-case basis;

Development and revision of guidelines, which will betemporarily limited to those guidelines that address an urgent public/animal health need or are necessary to support and facilitate preparations for Brexit;
Holding of non-product-related working parties, which will be temporarily reduced as a consequence of the scaling back of guideline development or revision;

Programmes and projects, where activities in relation to project governance will be reduced in line with the reduction/suspension of projects;

Organisation and attendance at stakeholder meetings, which will be limited to Brexit-related interactions;
Clinical data publication, for which the launch of new procedures will be temporarily suspended as of 1 August 2018; data packages submitted for medicines until the end of July 2018 will be processed and finalised.

The Agency added that detailed plans for the implementation of these measures are currently being developed and will be communicated to stakeholders concerned and the public as soon as they are available.

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