Innovate without sacrificing quality
Maintaining product quality in a rapidly growing, fiercely competitive regulatory environment is a challenge for even the most disciplined biotechnology organizations. Too often, technology becomes an inhibitor to innovation because it’s not flexible enough to be the enabler that it should be. This results in missed opportunities through process gaps and data falling through the cracks.
By adopting a no-code configuration technology, you can rapidly implement highly tailored solutions that fill gaps in your quality processes before they become insurmountable. That flexibility also means that as your business adapts and grows, so do the tools, so the software tail doesn’t end up wagging the business dog.
100% data coverage
Being able to capture whatever data is important to your business, from both desktop and mobile devices, then analyze and trend the results, means that nothing will get missed again, letting you focus on continuously improving.
Fully tailorable processes
With a no-code approach to application configuration, you can start small — say, by filling gaps in your existing QMS — then layer on more process flows as needed. And making changes later is as easy as point-and-click.
Field-level audit trails, workflow history, ad hoc reports, and automatic email notifications mean that everybody has visibility into what the system is trying to tell you — and those who are responsible can also be held accountable.