A new IT project called the Digital Application Dataset Integration (DADI) has been launched in the EU.
EMA has published Medical terms simplifier – a list of plain-language descriptions of medical terms commonly used in information about medicines.
On January 27, 2021, Fimea opened a website for adverse reaction reports for coronavirus vaccines. The page is updated more than once a week by the number and severity of adverse reaction reports.
Get to know the experts of our growing team. Welcome to Outi, Jaana, Katariina ja Soile.
EMA has launched a new OPEN pilot to increase international cooperation in evaluating COVID-19 vaccines and drug therapies. The project started in December 2020.
Fimea has approved the first notified body under the new Medical Devices Regulation (MDR), SGS Fimko Oy, in Finland.
Pharmacist specialising in industrial pharmacy Linda Tossavainen-Nikki, MBA and B.Sc. (Pharm.), and pharmacist Anna-Kaisa Tuderman, M.Sc. (Pharm), are joining our regulatory services team. Sami Tyrjy B.Sc. (Pharm.) has started as a new employee in our sales and marketing team.
Future trends were emphasised strongly in the discussion, especially with regard to the development possibilities introduced by new technological solutions. Read the highlights of the event.
DRA’s Market Access experts participate in the virtual ISPOR Europe 2020 conference. The theme of the four-day event is Improving Health: Establishing Incentives and Sharing Value. The aim of the event is to find new perspectives with the global network of HEOR experts on how we establish and share value sustainable for health systems, patients, and technology developers. Virtual ISPOR Europe 2020 will […]
Outi Järvinen, has started work as Head of Resourcing and Accounts in DRA’s sales and marketing team.
Get to know the experts of our growing team. Welcome to Pia, Virpi, Heli, Stina, Vilhelmiina, Riina and all three Heidi.