Our experienced team distills best practices to enhance the functionality of eCRFs. We simulate a paper-based CRF while ensuring ease of data entry. We help sponsors design accurate eCRFs that capture relevant data components during clinical trials, thereby saving significant time and effort.
Acceliant designs eCRFs that meet the unique requirements of sponsors. Our designers define data attributes such as enabling freeze, lock, and monitor while incorporating edit check specifications for seamless data collection. Our team consults the sponsor regarding systems, user interface, and other business rules at the client’s end for effective data collection across sites.
Acceliant understands that a clinical trial may undergo significant changes in protocol. Our designers manage eCRF version control and account for the shifts in protocol as well as edit check specifications.
We believe that the efficacy of eCRF design lies in successful deployment of the form. Our team undertakes validation of code list generation, form creation, edit check specifications, and performs user acceptance testing, at the sponsor’s request.