EMA publishes list of substances monitored by lead member states
A list of EU member states with lead responsibility for monitoring the safety of active substances has been published online by the EMA.
The European Medicines Agency (EMA) has published a list of active pharmaceutical substances for which individual member states will take the lead in monitoring.
Member states will be responsible for monitoring data on certain active substances that are contained in medicines, thereby optimising the use of resources across the EU bloc to protect public health.
For instance, the UK will monitor data on substances such as adenosine and alendronate, while Germany will take the lead on calcium and human albumin solution.
In cases where an active substance has not yet been assigned to an individual member state, all nations will be jointly responsible for monitoring its safety, the EMA confirmed.
The agency said in a statement: "This list of lead member states monitoring substances in nationally authorised medicines complements the signal validation work conducted by agency staff for centrally authorised medicines."
It added that the list will be updated online whenever a lead member state is identified for an active substance.
Experts hope that the work-sharing arrangement will help to identify any new risks associated with individual medicines.
Related News
-
News Introducing the Pharmaceutical Sustainability Ecosystem from CPHI
The Sustainability Collective from CPHI unveils the groundbreaking Pharmaceutical Sustainability Ecosystem to drive pharmaceutical knowledge sharing, connection, and collaboration in order to change the face of sustainability in pharmceutical... -
News US Government shutdown leads to the FDA grinding to a halt
The US Congress reached a deadlock after not being able to come to an agreement regarding funding, specifically reaching an impasse when Republicans and Democrats were unable to reach an agreement regarding Obamacare subsidies. The resulting shutdown o... -
News Biosimilars for the better: an expert view from Ecolab
Ecolab expert Renato Azevedo shares his insights on the current state of the biosimilars market in pharmaceuticals, after a high number of biosimilar drug approvals throughout the year confirming the shift of focus in this field. -
News US FDA announces new priority vouchers for accelerated review times
The US FDA announced a new priority program for drug developers – the Commissioner’s National Priority Voucher (CNPV) program aims to enhance the health interests of the US by allowing drug developers to redeem a voucher, shortening th... -
News CPHI Podcast Series: US drug policy – exploring the executive orders
The latest episode of the CPHI Podcast Series provides a timely overview of the recent policy changes in the USA, with President Trump signing excecutive orders to change drug pricing under a 'Most Favoured Nation' scheme.
-
News PhRMA trade association issues comments on Section 232 investigation
The Pharmaceutical Research and Manufacturers of America (PhRMA), an American trade association representing groups in the pharmaceutical industry, issued a letter on May 6, 2026 to the Department of Commerce regarding the Section 232 National Security... -
News Pharmaceutical Packaging Market Prospects: Shifting regional policies
The pharmaceutical packaging industry is experiencing significant transformation in 2025, driven by regulatory changes, supply chain challenges, and sustainability initiatives. The US BIOSECURE Act, passed through the House of Representatives in Septem... -
News The next 15 drugs up for negotiation with Medicare include several blockbusters
By now, everyone is quite familiar with the drug price negotiations taking place between drug companies and the Centres for Medicare & Medicaid Services (CMS) in the USA as part of measures being taken to reduce the cost of drugs for patients, to make ...