The EU Medical Device regulation is forcing medical device manufacturers to re-evaluate their clinical data strategy.
The need for a flexible industry specific EDC to reduce the workload and cost of clinical operations has never been greater.
SMART-TRIAL provides a full blown do-it-yourself EDC with supportive services, to help MedTech companies collect clinical data in compliance with industry regulations.
Cutting edge EDC for all MedTech companies
Designed to support all clinical activities
Simplifying MedTech regulation compliance
Empowering Clinical Teams to be their best
Without compromising on features, design, or compliance
What sets SMART-TRIAL apart?
The only solution that is tailor-made for Medical Devices
Medical Device Industry Experience
It's not only about features. As an EDC vendor we need to provide the right guidance on your clinical data strategy.
With over 8 years of experience working with various Medical Device manufacturers, we possess valuable know-how that we share with all our clients.
The SMART-TRIAL team provides both guidance and inspiration through articles, white papers, and project-based consultation.
Platform that Mirrors Industry Needs
Developed in close cooperation with clients and MedTech partners, the product team takes great pride in releasing four validated updates to SMART-TRIAL every year.
By implementing features that adhere to Medical Device manufacturers, we are building a long-term solution to fit the future of the MedTech industry and its regulatory framework.
EU MDR Compliance
SMART-TRIAL's goal is to become a part of the continuous clinical evaluation process and help you comply with regulations.
The platform, additional services, and licensing is designed to fit medical device life cycle activities.
Most EDC systems are designed for the pharmaceutical industry, which results in both costly and poor fit for MedTech.
Easy workflow with SMART-TRIAL
The easiest study setup you will ever try
Specify what data you want to collect
The way to group subjects together
Define what and when forms should be completedd
Subjects are enrolled and recruited to Sites