The only Quality Management Software designed to help MedTech teams deliver innovations to market, streamline compliance, and focus on quality — all in one end-to-end platform.
Greenlight Guru is the only modern, purpose-built solution to give MedTech companies an end-to-end system to manage the lifecycle of their product — all in one place.
Work on the most current version and save time with Part 11 compliant e-signatures, flexible review & approval workflows, and revision control.
Work on the most current version and save time with Part 11 compliant e-signatures, flexible review & approval workflows, and revision control.
Create detailed design control objects, link complex configurations, and attach documents with one click.
Create detailed design control objects, link complex configurations, and attach documents with one click.
Integrate quality and risk management into your design and development processes from the start.
Integrate quality and risk management into your design and development processes from the start.
Remain compliant and manage Nonconformances, Audits, and CAPAs throughout your product lifecycle.
Remain compliant and manage Nonconformances, Audits, and CAPAs throughout your product lifecycle.
Communicate where your team works. Avoid unnecessary meetings and emails by collaborating across apps.
Communicate where your team works. Avoid unnecessary meetings and emails by collaborating across apps.
Do more value-added engineering work and less compliance paperwork.
A connected quality ecosystem where every record of your QMS is organized, centralized, and traceable.
Empower your team with a software platform that accelerates device clearance timelines.