Deploy an EHR-integrated patient-reported outcomes (PRO) program designed to scale
Rapidly deploy clinical studies and registries on the EDC platform preferred by investigators
Unparalleled expertise to help you leverage outcomes data and meet your clinical and operational objectives
Streamline template management across multiple locations through a centralized hub
Optimize monitoring of enrollment progress and view real-time updates to confirm completion of informed consent forms
Adhere to strict regulatory standards like 21 CFR Part 11 for electronic signatures with the PatientIQ platform
A friendly user experience can help to maximize patient enrollment and participant compliance
A centralized management hub allows clinical researchers to keep studies moving forward on time
Learn the most common mistakes when conducting clinical research studies and how to avoid them to save both time and budget.
Healthcare Organizations
Healthcare providers
Patients
