Introducing the First European eClinical Suite for Medical Devices
With EU Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR) deadlines looming, BSI Life Sciences and SMART-TRIAL unite to offer an all-in-one, interoperable solution for medical device and diagnostics companies revising their clinical data strategy to ensure compliance and maximize resources.
Learn how the new MedTech eClinical Suite from BSI Life Sciences and SMART-TRIAL can advance your clinical trial.
Together, these two experienced, best-in-class companies, become the first European-based eClinical software suite specifically tailored to the MedTech industry.
The MedTech eClinical Suite from BSI Life Sciences and SMART-TRIAL ensures simplified and compliant clinical data gathering and management through enhanced oversight of clinical trials (CTMS), efficient study documentation (eTMF), and verified capture of clinical data (EDC).
Medical device manufacturers are in complete control of their studies and clinical data with the BSI Life Sciences and SMART-TRIAL MedTech eClinical Suite. This enhanced oversight helps MedTech companies streamline their clinical operations and simplify their path towards MDR and IVDR compliance.
Key features and benefits of the BSI Life Sciences and SMART-TRIAL MedTech eClinical Suite include:
- → Validated software with compliance templates
- → MedTech industry know-how and experience
- → European data protection
- → Simplified system management
- → Seamless system integration
If you work with a MedTech organization and have questions about how the technology-side of your clinical trials can be streamlined and more effective, or if you’d like to see our MedTech-specific platform in action, click here to get in touch with us.
