SMART-TRIAL uplifting study safety reporting for MedTech
New SMART-TRIAL Adverse Event reporting capabilities helps medical device companies comply with international standards and regulations on safety reporting in clinical studiesAalborg, August 17, 2020 SMART-TRIAL has deployed a new global release of its software to enable MedTech clinical teams to comply with international standards on Adverse Event (AE) Reporting, such as the ISO14155 and the Medical Device Regulation. This move is the first by any Electronic Data Capture vendor to provide in-built functionality directly tackling compliance requirements set forth by regulations and