The biggest mistake a company can make during the transition to postmarket is not having quality processes streamlined in advance. You need to have confidence in your CAPA, Audit, Nonconformance, and Complaint handling processes now. If you don’t, the consequences can be costly. Choose a QMS that supports your development and quality processes throughout your entire product lifecycle.
1,100+ of the world’s leading MedTech companies trust Greenlight Guru.
Quality Workspaces That Support Your Product Lifecycle
Keep your products on the market and ensure safety for your patients.
Your quality workspaces should have a framework to guide you. Whether it’s a CAPA or complaint, you and your team need to collaborate and strategize next steps.
Our quality workspaces enable you to work better with your peers. Assign tasks, link documents or design artifacts, create action items, investigate root cause, and generate critical documentation.
Your connected Greenlight Guru ecosystem gives your team visibility into the investigation.
Learn from the catalyst that caused the quality event to take place. Make your devices better and stronger with each update.
How Greenlight Guru Can Help
Uncover all of the ways our end-to-end solution built specifically for the MedTech industry can get you on the right track to prepare for regulatory submissions.