The recommendations include:
They are based on the analysis of the causes of shortages and regulators’ first-hand experience in coordinating the management of shortages, and industry associations have been consulted. The guidance has been developed by the HMA / EMA Task Force on the Availability of Authorised Medicines for Human and Veterinary Use. It complements the guidance for patients and healthcare professional organisations published last year. As medicine shortages can meanwhile be considered a global health problem, ensuring the availability of authorised medicines in the European Union (EU) is a key priority for EMA and the European medicines regulatory network.
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