Regulatory Technology

Moving beyond compliance

The reporting of regulatory clinical data has never been more befuddling—updates to retired, electronic and newly added measures complicate compliance, result in measurement gaps and leave leaders questioning the value of the data.

A proven market leader

With more than two decades of experience, our regulatory software within Q-Apps® was built to offer intuitive data capture, quality assurance; and action-oriented, on-demand analysis of new and custom measures.

The regulatory solution within the Enterprise Clinical Data Management (eCDM™) platform features capture and submission technology for core measures, plus market-leading reporting.

Optimize the efficacy of the software by combining it with the expert Q-Centrix team as a comprehensive solution.

How it works

Our solution offers high-fidelity data when it’s needed most and the detail you need to discover trends and insights.

Expert team captures clinical data

Aggregate and curate data within software

Deliver automated dynamic sampling of measured populations

Creates on-demand scorecards for trend monitoring and benchmark comparisons

Insights abound within the enterprise

  • Review and compare rates within one facility, or multiple, by a number of different factors to understand drivers of change.
  • Reporting options include compliance rate by measure set, for a focused approach, or by physician to understand individual performance.
  • Trending reports offer insights into current or future needed action.
  • Access insights into your measure set performance with a number of proven analytics including measure set status report, detail measure report, patient drill-down, and measure performance summary rate and trend reports.
  • Review and compare rates within one facility or multiple by a number of different factors to understand drivers of change.
  • Reporting options include compliance rate by measure set, for a focused approach, or by physician to understand individual performance.
  • Trending reports offer insights into current or future needed action.

“Support is very responsive to questions and issues. The team has always been prompt with regulatory changes and submissions of our data. The team provides very helpful education on regulatory changes.”

— Lead Clinical Database Specialist
1,000+ bed hospital in the Midwest

Q-Centrix experts

Lauren Gerstner

Senior Director, Product Operations

Bryan Wojnowski

Vice President, Strategic Initiatives & Regulatory Market