News - May 24, 2019

MDR: EUCOPE’s concern shared in latest Politico report

With almost one year to go before the implementation of the Medical Devices Regulation (MDR) 2017/745, the Brussels-based edition of Politico reports on the main problems for related stakeholders, whilst the European Commission is scrambling to get things in order… read more

News - May 22, 2019

EMA Regulatory Science Strategy 2025

You still have a bit more than one month to contribute to the EMA’s next strategy for regulatory science! The European Medicines Agency (EMA) is indeed seeking views from stakeholders, partners and the general public on its proposed strategy on… read more

News - April 26, 2019

MAP BioPharma Report on access to OMPs in the UK

Our member MAP BioPharma recently put forward a series of recommendations focused on UK’s appraisals and reimbursement processes, in their latest publication titled Access to Orphan Medicines: A Case for Change. The report shows that: Very small differences between treatments in… read more