Remote Possibilities: How Virtual Technology Is Changing Medical Device Investigations

Since the COVID-19 pandemic began, clinical study sponsors, investigators and the FDA have been increasingly accepting remote or virtual studies. While not all aspects of virtual clinical trials are conducive to medical device investigations, some elements may be incorporated.

Join Fox Partner Mark Yacura for a webinar on the regulatory, legal, clinical and practical aspects of virtual clinical studies for the MedTech industry.

Topics will include:

• Overview of remote clinical trials
• Differences and similarities between virtual and traditional studies
• Impact on the MedTech industry
• Investigational device exemption (IDE) in clinical studies, including the approval process and key considerations