Avicenna Alliance Observer at IMDRF meeting in Brussels
The Avicenna Alliance had received the honor to be invited as an Observer to the International Medical Device Regulators Forum (IMDRF) meeting taking place in Brussels on March 27 & 28. An unique opportunity to learn, inform, network and share the central role of modeling and simulation (in silico methods) for regulatory approval.
Although Digital Evidence is not yet a key topic for most of the presentations, many side conversations with Regulators, industry leaders and Non-Governmental Organization revealed the great enthusiasm and need to investigate and regulate In Silico outputs for complementing traditional evidence and improving the regulatory approval process while further increasing patient safety.
Let’s pursue our discussion in Berlin in September!