When: June 30, 2022 – 11:00am-12:00pm (EST)
*please register with company email if possible
Software in the medical device industry represents a rapidly expanding area in health care. The role of digital platforms continues to evolve and increasingly plays a vital role in all areas of a patient’s health, from diagnosis to treatment to monitoring.
As an integral part of medical devices, software may be used to manufacture a device, maintain a device or software itself can be a medical device. In all cases, the software needs to meet certain requirements and comply with the regulations; thus, it is important to determine which rules apply.