Research Related Injury and Medicare Secondary Payer Act Reporting Obligations

Screen Shot 2013-05-03 at 4.15.50 PM

Verified Clinical Trials offers Medicare Secondary Payer act compliance capabilities for clinical trials.  The trigger to initiate Medicare Secondary Payer Law  adverse events reporting and  ORMs (Ongoing Reporting for Medicals) is the date of incident of the research related adverse event or injury and NO payment or settlement is needed to initiate this required reporting.  The Verified Clinical Trials process captures the initial required information at screening.  Verified Clinical Trials have the expertise and tools to collect the necessary information, verify it’s accuracy, and store the information.  The clinical research sites do not have the tools required to obtain nor safely store this personal identifying information.

Verified Clinical Trials are experts in clinical research, Medicare billing, and collection and verification of personal information.

 

Leave a Comment