On May 31 you are welcome to the Discusssion ”Equal care for all – progress and priorities in the treatment of rare disease patients”.
The participants of discussion will debate proposed review of the European Union regulations on rare desease drugs and paediatrics, as well as the new Latvian Plan in the field of rare diseases, that has been under discussion for a year. The experts will discuss the progress made in recent years in improving the treatment of rare diseases and the priorities for the coming years.
Experts from European Union institutions, members of the Rare Diseases Support Group in the Saeima, members of the Saeima, representatives of the Ministry of Health and the National Health Service, specialist doctors, patients ‘associations, manufacturers’ associations and the media are invited to participate.
Please register: https://lnkd.in/dimWCZ3h
Online: LA.LV ; https://lnkd.in/dUxzJed6