Regulatory Affairs

The TREAT-NMD Regulatory Affairs Database is a valuable source of advice to people who are involved in the planning of mono- or multi-centre clinical trials within different European countries.
The current version contains the contact addresses of national authorities as well as national legislation and documents from  11 European countries.

Additionally, European regulations and other important international documents and guidelines are provided (e.g. from ICH and EMEA).

The database is open for public use and can be accessed online, a login/username is not required:

www.treat-nmd.eu/regulatoryaffairs

If you can provide the CTCC with valuable sources of information or contact persons regarding the legal regulations in your country please contact us. We also welcome any technical suggestions. Your help would be very much appreciated and further accelerate the development of this valuable database.

For technical issues please contact

For content please contact