The MedTech eClinical Suite from BSI Life Sciences and SMART-TRIAL ensures simplified and compliant clinical data gathering and management through advanced oversight of clinical trials (CTMS), efficient study documentation (eTMF), and verified capture of clinical data (EDC).
“By bringing together our two experienced, best-in-class companies, we become the first European-based eClinical software suite specifically tailored to the MedTech industry,” explains Jan Nielsen, Community Manager, Life Sciences at BSI. “We’re very pleased to be partnering with SMART-TRIAL on this flexible, unique, and much-needed solution.”
Medical device manufacturers are in complete control of their studies and clinical data with the BSI Life Sciences and SMART-TRIAL MedTech eClinical Suite.
“Clinical teams are under pressure to deliver more evidence than ever before. This requires thorough control and oversight of every single activity that produces clinical data,” says Jon Bergsteinsson, VP of Global Business Development at SMART-TRIAL. “The partnership between SMART-TRIAL and BSI Life Sciences is designed to help MedTech companies streamline their clinical operation to simplify the 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
SMART-TRIAL helps MedTech clinical teams comply with regulations on clinical evidence by simplifying the collection and management of data. Tailor-made for MedTech, SMART-TRIAL offers a do-it-yourself electronic data capture for clinical investigations, clinical performance studies, PMCF, and PMPF activities, including registries, surveys, and case-series.
SMART-TRIAL is built to empower clinical teams to be their best, and in full control of their data, without compromising on features, design, or compliance.