MyVeeva is a new application for clinical research sites that makes it easier to deliver a patient-centric and paperless clinical trial experience.
With capabilities for eConsent, virtual visits, patient adherence, and ePRO, MyVeeva gives sites more flexibility and makes it easier for patients to participate in clinical trials.
MyVeeva for Clinical Trials is free for clinical research sites and is planned for availability in January 2021.
Improve Patient Enrollment and Retention
Collaborate with patients remotely to reduce patient burden and improve satisfaction.
Streamline the Collection of Clinical Trial Data
Reduce redundancy and simplify the delivery, collection, filling, and storage of patient-related information.
Free for Sites
Engage virtually with your patients across all of your studies at no cost with a system that you own and control.
MyVeeva for Clinical Trials is Planned to Include:
Easily share information and collect patient consent electronically with less time and effort. Allow patients to use their own device to provide consent for improved convenience
Collaborate remotely with HIPAA-compliant audio and video capabilities, allowing seamless communication between sites and patients.
Replace paper questionnaires by allowing patients to report on treatment outcomes electronically, from their own mobile device.
Help patients take medications and adhere to their treatment regimens. Send reminders to patients about study activities to support protocol compliance.
Integrate with Veeva SiteVault
Connect seamlessly with Veeva SiteVault to reduce redundancy across studies and patients.
"Having the ability to conduct parts of a study remotely is key to a better patient experience and speeding study conduct. It’s a crucial shift for the industry and I appreciate the innovation Veeva is bringing to this important area.”
Program Director for Investigator-initiated Clinical Trials | Vanderbilt University Medical CenterRead More