Category: Medicines

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The future of medicated feed

The future of medicated feed

A proposal for a Regulation of the European Parliament and of the council on the manufacture, placing on the market and use of medicated feed and repealing Council directive 90/167/CEE was presented by the European Commissionin 2014 and it is now in the later stage for approval. The proposal legislation aims to regulate the manufacture, […]

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Keeping medicines safe

Keeping medicines safe

How EMA monitors medicines once they are on the market After its authorization a medicine is used by many patients, often together with other medicines. After some time, certain side effects may emerge that have not previously been identified because no medicine is a 100% safe. It is therefore essential that the safety of all […]

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Are pharma companies prepared for Brexit?

Are pharma companies prepared for Brexit?

The European Medicines Agency (EMA) and the European Commission are currently providing guidance to help pharmaceutical companies responsible for medicines to be prepared for the UK withdrawal from the EUwhich will become a third country as of 30 March 2019. The objective is to ensure that companies are ready to take the necessary steps to enable undisrupted supply of their medicines […]

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EMA prepares for Brexit

EMA prepares for Brexit

Business continuity plan aims to preserve Agency’s ability to protect public and animal health The European Medicines Agency (EMA) has developed and initiated a business continuity plan to deal with the uncertainty and workload implications linked to the United Kingdom’s (UK’s) withdrawal from the European Union (EU) and the Agency’s relocation. The business continuity plan is a […]

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