Is Europe prepared to assess medicines based on new technologies or novel innovations, or different types of study data?
Meet us at the TOPRA Annual Symposium on 30 September – 2 October 2019 in Dublin, Ireland.
EMA has published guidance to marketing authorisation holders and authorities to improve and harmonise management of medicine shortages and related reporting and communication.
The expert event brought together more than 50 representatives of the pharma industry and medicinal wholesalers to exchange experiences and thoughts on how to control availability of medicines.
Pauliina Lajunen will help boost DRA’s growth and internationalization with her business and marketing expertise. Welcome Pauliina!
Availability of risk management materials and electronic systems were much-discussed topics at the traditional pharmacovigilance seminar in Oslo.
Our big team has grown even bigger! Welcome three new colleagues, Heidi, Heli and Tuomas!
Medicines verification to deter falsified medicines will be implemented as of 9 February 2019. Are you ready?
This information means that a great number of new translations and variations will be needed, so start preparing your action plan already now.
Do you write pharmaceutical articles, reports or expert opinions? Or do you perhaps produce multi-language video tutorials or applications for patients?
We can help you with all of these.