Rule 23-225-2.6 - Documentation The provider must document the remote patient monitoring service the same as for a comparable in person service which includes, but is not limited to:
A. The monitoring equipment meets all of the following requirements: 1. Capable of monitoring any data parameters included in the plan of care, 2. Food and Drug Administration (FDA) Class II hospital-grade medical device, and 3. Capable of accurately measuring and transmitting beneficiary glucose and/or blood pressure data. B. Qualified staff installed the remote patient monitoring equipment necessary to monitor and transmit the data according to the beneficiary's care plan. C. Clinical data was provided to the beneficiary's primary care physician or his/her designee. D. Monitoring of the beneficiary's clinical data was not duplicated by any other provider. E. Beneficiary's home environment has the necessary space and connections for installation and transmission of data.23 Miss. Code. R. 225-2.6
Miss. Code Ann. § 43-13-121.