Greenlight Guru Clinical has been designed to support post-market activities for MedTech since its first release back in 2014. Collect data to comply with the In-Vitro Diagnostics Regulation (IVDR) on PMPF.
Whether you need to conduct an analytical or clinical performance study, you have all the tools you need to collect and oversee your PMPF data.
Greenlight Guru Clinical's tools are used by both large and small MedTech companies to collect data on clinical performance - all over the world.
What PMPF activities have you planned?
Design custom eCRFs or data forms with automatic rules and validation.
Collect data directly from subjects and keep them engaged via email and SMS.