eVERA is cloud based pharmacovigilance platform that captures, processes, and analyzes adverse events, with the ultimate goal of providing our primary business customer, the manufacturers, with abundant real-world evidence, enabling a better understanding of the benefits and risks of their products.
Collecting adverse drug events from healthcare professionals and the public is mandatory for manufacturers. Minimum criteria apply to make such a case report valid. A valid
Some adverse drug events are a predictable consequence of therapeutic, especially dosing failures. Idiosyncratic toxicities, on the other hand, are much less predictable and much more
Some medications are administered as prodrugs that need to be metabolized in the active form by the body. An example of such a drug is codeine.
Medical Devices Regulation 2017/745 and In Vitro Diagnostic Medical Devices Regulation 2017/746 The new European legislation places numerous new obligations on manufacturers of medical devices marketed
Medical Devices Regulation 2017/745 and In Vitro Diagnostic Medical Devices Regulation 2017/746 U.S. manufacturers of medical devices who are placing their devices on the European market