The NetPRO™ System – Bringing ePRO to Every Internet User Worldwide

NetPRO is a browser-based method for PRO data capture that sends data to a central server and database for web review by site and sponsor.

Regulatory agencies encourage sponsors to collect data directly from patients. Clinical professionals are eager to leverage the Internet to collect patient-driven eDatathese ePRO data for large clinical studies and post-market surveys.

ePRO on the web helps sponsors collect faster, more efficient data to help the clinical research industry develop new therapies, treat disease and improve quality of life.

NetPRO is ideally suited for late phase research and is cost-effective for large studies with long durations. By using a web browser to host the diary or questionnaire, NetPRO can collect ePRO, eCOA, and post-marketing safety data from large global populations. PRO data collected with NetPRO can support a labeling claim.

NetPRO includes the PHT’s secure backend server and StudyWorks™ for easy data management by sites and sponsors.

NetPRO provides more options to sponsors for collecting ePRO. NetPRO is 21 CFR Part 11 compliant and a member of the same PHT ePRO system sponsors have used on over 600 trials.

Patients use NetPRO on any device that connects to the Internet including smartphones, tablets, desktops and netbooks. By leveraging patient technology researchers can access thousands of patients, reducing the costs of large Phase 4 and extended post-market studies.

Key NetPRO Features & Benefits:

• A larger screen size compared to other ePRO platforms makes it easy to use. The layout is similar to paper, possibly reducing amount of validation work required for electronic questionnaire. Text abbreviations are eliminated.
• Uses patient’s own technology – NetPRO offers enhanced ease-of-use and simplicity with familiar technology and easy availability at both the site and patient’s location. Users gather highly compliant ePRO data without an investment in hardware of any type.
• Progress bars illustrate progression through the questionnaire to encourage high compliance and fewer patient drop-outs to reduce missing data.
• Restricted time response windows deliver timely and verified data entry with no unplanned recall bias or prospective responses.
• Accurate timestamps ensure confidentiality assurance, eliciting honest patient answers
• Custom branding on questionnaires and data review portal increases brand exposure to target patients and clinicians.