OIG’s Call for Increased Oversight of Remote Patient Monitoring Misses the Mark

Learn about the Office of Inspector General’s new report around remote patient monitoring and the key areas where it misses the mark.

FDA Issues Final Guidance on Clinical Decision Support Software and Software as a Medical Device: Key Takeaways and What it Means for Digital Health Companies

Michael SchellhousOctober 11, 2022SaMD, clinical decision support software, software as a medical device

Tips on a Successful 510(K) Submission for Smaller Companies

Remote Monitoring, FDAMark Mansour, Esq.January 13, 2022medical device, software as a medical device, Remote Monitoring, FDA, 510(k), medical device approval pathway

How RPM Companies Can Leverage the New Remote Therapeutic Monitoring CPT Codes Expected in 2022

With these new RTM codes set to go into effect January 1, 2022, RPM vendors already in the remote monitoring arena should start preparing now for how they can take advantage of this new reimbursement opportunity.

[video] Digital Health Innovators: Does your solution qualify as Software as a Medical Device (SaMD)?

If you’re in the Remote Patient Monitoring (RPM) or Remote Therapeutic Monitoring (RTM) space, then you’ll want to understand the criteria and opportunities for qualifying as Software as a Medical Device (SaMD)

What You Need To Know

Who We Are

Who We Serve

The Latest

Contact

Get Started

Nixon Gwilt Law
216 Apple Blossom Court, Suite 200
Vienna, VA 22181

What You Need To Know

Nixon Gwilt Law216 Apple Blossom Court, Suite 200Vienna, VA 22181

Nixon Gwilt Law
216 Apple Blossom Court, Suite 200
Vienna, VA 22181