News

EFPIA survey highlights medicines issues

Amy Schofield 09 November 2017

EFPIA has published results of a survey underlining the scale and importance of the medicines issues that it says must be addressed as part of the Brexit discussions, in order to protect public health.

The survey highlighted that medicines used by patients across Europe have integrated supply chains, which include the UK:

• Over 2600 final products have some stage of manufacture based in the UK
• 45million patient packs are supplied from the UK to other EU-27/EEA countries each month
• Over 37million patient packs are supplied from the EU-27/EEA to the UK each month.

In this context, 45% of EFPIA members expect trade delays if the UK and Europe fell back to WTO rules. To prevent these delays, critical for patients to access their medicines, the EU and UK should agree a comprehensive agreement that ensures maximum alignment between EU and UK pharmaceutical laws.

In addition, over 12,000 centrally authorised Marketing Authorisations (MAs) for medicines will require a separate MA in the UK in order for the medicine to be prescribed to patients. Approximately 17% of centralised MAs are held in the UK.

There are over 1500 clinical trials being conducted in multiple EU member states that have a UK-based sponsor. Over 50% of these trials are scheduled to continue beyond March 2019.

The figures from the EFPIA survey underline the importance of scientific research collaboration between the UK and EU, which strengthens the EU’s global position in life sciences and attracts global life science investment to the EU.

Commenting on the survey, EFPIA Director General, Nathalie Moll, said: “The survey underlines the scale of the task ahead. For life saving and life improving medicines, the EU and UK cannot afford to wait any longer to ensure that the necessary cooperation on medicines is in place from the day the UK leaves the EU.

“Even in the context of the Brexit negotiations where all sectors are looking for clarity on the future, it is important to recognise that the medicines sector is different. The medicines we make impact directly on peoples’ health. Securing ongoing cooperation on medicines regulation between the UK and EU is the best way of ensuring that patients across Europe continue to have access to safe and effective medicines.”

 

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