
With the extraordinary rate of change in the medical device industry and requirements for ISO 13485, it can be difficult to keep up with the required documentation.
iPassport can help by automating the simple yet time-consuming tasks for you; document actions can be automated through workflows ensuring that the correct people are notified at the correct time. You can also create risk assessments as benchmarks, review with product development and link to associated nonconformities, update associated documentation and link back to the risk assessment.
It simplifies processes, leaves a clear audit trail and helps you to streamline your processes – saving you time and money.
Modules
iPassport provides a complete suite of quality management modules, allowing you to easily keep on top of everything from document control to staff training.
Why choose iPassport?
iPassport is trusted by laboratory and quality managers at some of the world’s best known healthcare and research facilities. Continually improved and refined since its launch in 2007, we are widely acknowledged as a leader in our field.
Easy to use
Our intuitive system can be easily integrated into your ways of working.
Meet requirements
Functionality designed to give you the smoothest pathway to accreditation or certification.
Web-based system
Access 24/7 from any location, no local IT support or installation required
Managed
Continual system improvements including new features, modules and architectural enhancements.
Secure
Robust encryption and controls; 99.9% uptime guaranteed as part of SLA
Cost effective
Reduce admin time and eliminate paper; all modules included as standard