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?
Learn how Oticon A/S has streamlined their verification & validation testing to comply with the MDR.
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Learn how Elminda is using Greenlight Guru Clinical to collect data in post-market clinical studies.
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