Case Study: Timely Communication within Clinical Trials is Essential for Success
Learn how effective use of text, notifications, email, fax, reports, and alerts enable us to connect with hundreds of clinical study participants and personnel.
Learn how effective use of text, notifications, email, fax, reports, and alerts enable us to connect with hundreds of clinical study participants and personnel.
IVRCC's custom-built native app was an ideal choice for the Operating Room that had no access to Wi-Fi, by being able to accommodate a large number of Inclusion/Exclusion criteria, the possibility of tablet or internet failure, and proper randomization treatment assignment exactly per protocol.
The client compared the costs of our BYOD system with two other bids which collected data from subjects using proprietary handheld devices. With our IVR system, patients use their own phone or smartphone for daily diary collection, which saved the client several hundred thousand dollars.
IVRCC collaborated with the client on a multi-center, randomized, double-blind, parallel group, vehicle-controlled study. The client realized a significant cost savings by combining two protocols, IRT application build, validation, hosting and maintenance costs into one application.
Learn how our ePRO applications created a successful Seasonal Allergic Rhinitis Therapeutic Equivalence Study.
From project managers to administrators and programmers, the IVRCC team worked closely with the client to design and create custom applications that tracked and displayed the results of diary compliance to the participants. All calculations were in real-time so that the system reporting was current and accessible at all times.
IVRCC was able to provide an affordable and adaptable solution that provided data that was easy to integrate with the final EDC database. The study article was recently published in The New England Journal of Medicine.
Find out how our automated supply management resulted in less work and better inventory control. The objective of this study was to evaluate the safety, tolerability and efficacy on subjects with opioid-induced constipation. Clinical trial materials management services provided by IVR Clinical Concepts were a key component to the success of this study. Patients were provided kits which included medication and a Bristol Stool Scale.