A new LuminLogic for a new (virtual) world

We’re all continuing to adapt to the virtual modifications required by today’s novel reality. Even as some states work to “open up” businesses, most of us still remain in web-collaboration mode.

Since the start of the COVID crisis, MethodSense has been diligently focused on evolving our recently released LuminLogic 6.0 software to accommodate medical device companies within a virtual compliance environment. To that end, we are excited to announce the release of LuminLogic Version 7.0, a 21 CFR Part 11 compliant SaaS solution that supports document, regulatory, quality, and risk management systems for the compliance efforts of medical device and other life science companies.

LuminLogic 7.0 includes a new wave of functionality in support of our clients’ compliance efforts, including complaint management, corrective action/preventive action (CAPA) management, and training management. Plus, we’ve extended the software’s highly intuitive interface and modular flexibility for significant functional enhancements.

LuminLogic 7.0 benefits

  • CAPA creation and assignment
  • Customer complaint and training documentation
  • User notifications for high-impact engagement
  • E-signature capability for task completion/compliance documentation
  • Auditability to ensure compliance under regulatory scrutiny

Regardless of their size or the extent of their virtual operations, our clients will benefit from the innovative updates we’ve made to this product. As remote offices and online operations are anticipated to be the new norm, LuminLogic 7.0 is a critical necessity for compliance management.

This website uses cookies and asks your personal data to enhance your browsing experience.