Dear European Medicines Agency,

Under the right of access to documents in the EU treaties, as developed in Regulation 1049/2001, I am requesting documents which contain the following information:

'Applications for new human medicines under evaluation by the CHMP'.

I am aware that these documents are published on the EMA website dating back to March 2012. I have been informed by personnel at the EMA that before this time these documents were not posted online.

However, I am emailing to request files regarding the applications for new human medicines under evaluation by the CHMP, which contain a list of applications for centralized marketing authorization for human medicines that the EMA has received for evaluation. I am looking for the documents with the international non-propriety names and therapeutic areas for all new medicines under evaluation by the CHMP.

I am looking for this information regarding non-orphan medicinal products, non-orphan generic and biosimilar medicinal products and orphan medicinal products.

I am requesting the documents holding this information starting from February 2012 (following the last available file online) and as far back as possible that the EMA holds. As I understand from the documents currently available online these are usually files dated monthly. If this is not possible I would like to request the information, more specifically, for the period of February 2012-February 2007.

Yours faithfully,

Lucie Ellis