Ensuring Lab Compliance Through Simpler Documentation

Typical lab documentation is often created and maintained by subject matter experts and other medical professionals who are not trained writers. Most content is dense and inconsistent, and difficult to use, comprehend and follow in the field.  

The biggest risks from poor documentation are:

  • non-compliance with CLIA quality standards, and
  • FDA, CDC, CMS, and/or CAP inspection.

Are your procedures inspection-ready?

In this webinar, you’ll learn how our research-based Methodology standardizes and simplifies SOPs and other critical documentation to improve compliance between what's documented and what's actually done.

Download this free webinar to learn more.