Author: verwaltung

As Switzerland is not a member of the European Union, it is not obliged to implement European legislation into national legislation. Instead, different laws and regulations of the Federal Council and the Agency Council are to be applied when dealing with drugs and medical devices. With regard to clinical research, this article deals with the…

When preparing submissions for medicinal products for human use, the most important question that sponsors, study nurses and CRAs need to answer is which German authority is responsible for processing their application. Especially, if it is the first time that you are in charge of a submission you might be in doubt as to whether…

Europe´s second largest trade show in medical technology – the MedtecLIVE – was hosted in Nuremberg between May 21st and May 23rd. MEDICRO also participated as one of the exhibitors and we are gladly looking back on three overwhelming days full of promising conversations and new contact possibilities. We would like to thank our visitors…

MedtecLIVE is the result of a merger of Medtec Europe and MT-CONNECT. With approximately 350 exhibitors it is Europe’s second-largest exhibition for medical technology. From 21 May to 23 May 2019, MEDICRO will be participating as a direct exhibitor at the MedtecLIVE, which will take place at the Exhibition Centre Nuremberg, Germany. You can meet us in hall 10,…

Recording, reporting and evaluating side effects during clinical trials on drugs and after the drugs’ marketing authorisation is imperative for the safety of patients. With medical devices, too, patient safety has priority. Unlike with drugs, though, the safety of users and third parties is also recorded here. This article shall highlight the differences between an…