Regulatory News

Publication of clinical reports: EMA adopts landmark policy

The European Medicines Agency (EMA) has decided to publish the clinical reports that underpin the decision-making on medicines. The policy will take effect from 1 January 2015.

Read the full statement from the EMA

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Information on suspected side effects now available through a single website

Information on suspected side effects, also known as suspected adverse drug reactions, of an additional 1,700 active substances contained in medicines approved in the European Union (EU) are now available through a website maintained by the European Medicines Agency (EMA), www.adrreports.eu

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Human medicines highlights - Issue 67 - September 2014

The September 2014 issue of the European Medicines Agency's newsletter 'Human medicines highlights' is now available.

All issues of the newsletter are available on the Agency's website.

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Human medicines highlights - Issue 66 - August 2014

The August 2014 issue of the European Medicines Agency's newsletter 'Human medicines highlights' is now available.

All issues of the newsletter are available on the Agency's website.

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Human medicines highlights - Issue 65 - July 2014

The July 2014 issue of the European Medicines Agency's newsletter 'Human medicines highlights' is now available.

All issues of the newsletter are available on the Agency's website.

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