View this webinar to learn how staicy can integrate seamlessly your internal and external clinical applications and utilize her proprietary functionality to uniquely select geographical storage location for your data.
The new EU Medical Device Regulation (MDR) was officially passed in May 2017 and manufacturers now have until 2020, to be fully compliant with all changes set forth within the new regulation. View this webinar to better understand the changes that clinical affairs teams should prepare for now to be successful under the new regulation.
Whether you are a first-time inventor with a novel idea emerging from an unmet need in patient care or a large manufacturer with a rich history in bringing medical devices to the market, the thrill of being at the forefront of an innovative concept is both exhilarating and overwhelming. The development of a successful medical product not only requires optimized engineering design efforts, but also clinical, regulatory, marketing and business expertise.