Choose the product that fits your needs
GCP compliant data collection for PMCF & market analysis.
Learn more about CasesLearn more about SurveyRequest pricing for your PMCF plan or clinical investigation
TALK TO SALES
All-you-need eCRF for pre orpost-market clinical studies.
Collect data directly from subjects with BYOD improve patient experience.
GCP compliant survey-based data collection for PMCF or market analysis.
Fully integrated eCRF & ePRO for clinical studies.
Learn how Oticon A/S has streamlined their verification & validation testing.
Our customer success team will help you take the first step in using the platform. From there on, you can setup and manage studies in SMART-TRIAL all by yourself.
SMART-TRIAL Onboarding is mandatory for all first time licensees and includes consultancy and training to ensure GCP compliant study set-up and to reduce the time of implementation.
SEE OUR REFERENCESA new initiative for early-stage MedTech companies
Level the playing field and get access to the same resources as your established peers.
MedTech clinical operations are as different as they are many
Nobel Biocare has implemented SMART-TRIAL for data collection in several clinical research projects of different complexities. We are pleased with the intuitive and straightforward setup of new projects and the great usability in data collection. Moreover, we are very grateful for the fast and helpful support from the SMART-TRIAL team when it comes to flexibility towards project setup and ideas for facilitating processes.
SMART-TRIAL will enable our many clinical specialists to better collaborate, interact and speed the collection of clinical evidence.
ElMindA is a data-driven company and constantly aims to improve the quality and visibility of data. We believe that the SMART-TRIAL data management platform will help us to achieve these mandatory goals.
Oticon's mission is to continue delivering the best hearing aids in the world. And we believe that SMART-TRIAL can help us doing this faster than we have done before.
SMART-TRIAL’s disruptive cloud technology helps Quanta’s clinical trial teams to work faster and significantly reduce the costs of generating and managing clinical and operational data, from our perspective, it is transforming our extended data ecosystem.
With SMART-TRIAL we have the opportunity to collect and manage our post-market data from all over the world in one place. The email and SMS reminders help with the timeliness of responses and, after a study ends, the data can straightforwardly be downloaded. Whenever we are in doubt about anything, support is friendly, efficient, and fast.
Due to the sensitive topic and the large target size, we had high demands on both security and usability. We believe we made the right decision by selecting SMART-TRIAL, because it meets our requirements for both compliance and a user-friendly interface.
