Virtual Clinical Trial : study design and administration support
Adopting electronic patient-reported outcome study designs can be daunting for sponsors who are used to traditional site-base studies. Without proper support, this can lead to suboptimal protocol design and trial failures. For remote data collection studies, Healint works closely with clients to develop the ideal decentralized trial design that is adapted for smartphone format while ensuring industry-leading study completion rates.
Smooth execution
We bring our cross-functional UX, marketing insights to ensure smooth execution of fully virtual and hybrid studies.
Our services include (à la carte):
Co-Develop protocol/synopsis
Protocol review
Suggestion on best approach to outcome measurement
Co-Author future protocol amendments
Develop internal project communication plan
Draft Informed Consent Form(s) (ICF)
Develop and Test online ICF(s)
Deploy and maintain ICF(s)
Revise ICF/PRO based on protocol amendments
Study preparation progress reporting
Detailed planning. Overview of the clinical study plan
Studies for phase 2, 3 or 4. Development and medical affairs studies.
All our services are preconfigured to be used off the shelf. Upon request, they can be customized to specific needs. They help our clients to save time and budget.