See how it works



Standardized PCR software



A fully validated software 


CE-IVD certified

FastFinder is certified as an in vitro diagnostics tool according to Directive 98/79/EC.


Manufactured in an ISO13485 setting

UgenTec's quality management system is certified with ISO13485 Medical Device Quality System.


Built to comply

- IEC 62304:2006
- ISO 14971:2007
- IEC 62366:2007
- Directive 98/79/EC 


Safe and sound in the cloud

All your data is kept in a Microsoft Azure supported cloud-environment. Microsoft Azure is one of the fastest, most secure & fully certified cloud platforms available..

Features to standardize your workflow

audit trail.png

Full audit trail

Unique user logins allow you to track every edit or approved result back to the right person. 


Off-site validation support

Get support from UgenTec's QA-team. We'll provide you with the documents needed to implement FastFinder into an ISO15189 regulated setting.


Separate validation environment

Software upgrades will never interrupt your routine workflow. With FastFinder Accept, we provide you with an extra environment, entirely dedicated to validation & testing.


Multiple laboratories, one standard

Multisite laboratories can use one software, resulting in a standardized PCR-protocol even on different devices.

Ready to get started?
Get in touch with our product experts to find out how a standardized PCR workflow can help you.

See how it works