23 June 2016 - The EMA has published a monthly statistics report on the medicinal products for human use that have been reviewed by the agency for the year to date.
The document provides current information related to the volume and evaluation of marketing authorisation and post-authorisation applications for medicinal products for human use received by the EMA.
The purpose of the report is only to provide ongoing factual information. Commentaries and analysis are provided in the Agency's annual reports.
As at May 2016, the agency had started 27 marketing-authorisation applications and had finalised 26.
For more details, go to: http://www.ema.europa.eu/docs/en_GB/document_library/Report/2016/06/WC500209286.pdf