The European Medicines Agency (EMA), in collaboration with the European Commission (EC), has established a standard procedure for manufacturers of certain high-risk medical devices to request ...
The European Medicines Agency (EMA) has approved an additional 2 mL pre-filled pen option for subcutaneous administration of Takeda’s Takhzyro (lanadelumab), aimed at treating hereditary angioedema ...
The European Medicines Agency (EMA) said Monday it has established a way for manufacturers of certain high-risk medical devices to request scientific advice. Manufacturers of class III devices and ...
Due to the generous grant provided by the Southern Ohio Medical Center Development Foundation and the efforts of Scioto County Emergency Management Agency Deputy Director Bill Lynn, Scioto EMA ...
EMA, in close collaboration with the European Commission, has established a standard procedure for manufacturers of certain high-risk medical devices to request scientific advice on their intended ...