EU-wide task force publishes work programme 2019/20 and prepares multi-stakeholder workshop
The task force set up by European Union (EU) regulators to better address potential problems with medicines’ supply and to avoid shortages published today its work programme for the coming two years. Improving the availability of human and veterinary medicines authorised in the EU is a key priority of the EU Network1. The work programme lists actions for regulators and industry alike to ensure the availability of medicines for the benefit of patients in the EU.
The task force has been set up by the European Medicines Agency (EMA) and the Heads of Medicines Agencies (HMA), with representatives from the European Commission and interested national competent authorities, the chairs of the Co-ordination Group for Mutual Recognition and Decentralised Procedures – Human (CMDh) and Veterinary (CMDv), the GMP/GDP Inspectors Working Group, the Working Group of Communication Professionals (WGCP) and the European Surveillance Strategy Working Group (ESS WG).
The task force will develop and coordinate actions for better prevention, identification, management of and communication on issues that can affect the availability of medicines, in order to improve continuity of supply of human and veterinary medicines across Europe.
Key priorities of the task force include:
The task force will organise a multi-stakeholder workshop on 8-9 November 2018 to gather stakeholders’ perspectives on how to address availability issues and to include their input into the deliverables of the task force. It will bring together all stakeholders impacted, including patients, consumers, healthcare professionals, industry, wholesalers/distributors, parallel distributors, academia and regulators.
The withdrawal of the United Kingdom from the EU is also likely to affect the availability of medicines in the EU. In this context, the task force provides a platform to facilitate and coordinate actions between Member States, EMA and the European Commission.