Core Registry Subscription

A longitudinal clinical registry tracking the outcomes and activities for RA and PsA patients. Utilizing data collection forms developed in concert with noted thought leaders. The size and detail of the data allows for questions to be addressed that would otherwise require significant investment in time and resources.

The data collected is able to stay current with new product launches and treatments by revisions to the forms as needed.

The number of queries that can be submitted is unlimited. Bio-statistical service hours are allotted on a quarterly basis but can be contractually expanded or added on an ad hoc basis, depending upon anticipated utilization.

Demographics of the database are available upon request.