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The European Medicines Agency (EMA) evaluates an increasing number of new cancer medicines. EMA collaborates with the European medicines regulatory network and international regulators to address the unmet needs of cancer patients. This is meant to advance cancer care and alleviate the burden of cancer in the European Union (EU). It is in line with...
A risk minimisation measure (RMM) is intended to reduce adverse reactions of medicines, also called side effects. These measures and the risks they address feature in the product information of medicines authorised in the European Union (EU). Where needed, these measures may also feature in additional resources. The European Medicines Agency (EMA)...
Patients can locate trials for potential enrolment in their area
The European Medicines Agency (EMA) publishes information on medicine shortages that affect or are likely to affect more than one European Union (EU) country, where it has assessed the shortage and provided recommendations to patients and healthcare professionals.
Members of EMA scientific committees and NCAs assessors who work with scientific advice procedures are invited to attend this webinar to learn how Scientific Explorer can help them in finding relevant information easier and faster.