A CE-mark is not enough to bring medical device products to the market. Claudia Wild, EUnetHTA member, talks on synergies between medical device regulation (MDR) clinical evidence demand and synergies with HTA processes at the MedTech Access Leaders Forum in Berlin Dec 3-5, 2018. Read more about the event here: https://lnkd.in/gGnXfp5
New publication: Finasteride treatment and male breast cancer: a register-based cohort study in four Nordic countries.
By pooling Nordic health data on medical devices & pharmaceuticals, and analyzing it on the micro-level, we tap into the full potential of big data. The Nordic health registers cover 26 mill. people from birth to death. Read about our most recent safety study, pooling data from 4 Nordic countries, here: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5773955/