MethodSense Completes CAPAs, Complaints, Training and Project Management Improvements to LuminLogic Version 7.0

Mar 04, 2021 Mark

Press Release ( - MORRISVILLE, N.C. - Mar 04, 2021 - MethodSense, Inc., a medical device-consulting firm, announces new system and project management improvements to its LuminLogic 7.0, a 21 CFR Part 11 compliant SaaS solution that supports document, regulatory, quality, risk-management, and project management for the efficient management of medical device and other life science company compliance efforts. These improvements are available immediately.

System improvements include auditable Corrective Action/Preventive Action (CAPA) and Complaint management functionality, from issuance to close, with global search option throughout the system; multiple document upload; regulatory training functionality with ability to create training assignments and monitor progress and completion; enhanced E-signature capabilities; and additional notification and reports throughout the system.

Additionally, a few of the many more administrative improvements feature secure, password-protected bulk document download and enhanced Timesheet Reporting for managing multiple projects and tasks in one report to enable project managers to create enhanced project reporting.

“These improvements to the functionality of LuminLogic 7.0 and its highly intuitive interface and modular flexibility underscore our continued commitment to support our clients’ compliance efforts in the face of regulatory scrutiny,” says Rita King, MethodSense CEO. 

“MethodSense’s clients, regardless of their size or the extent of their virtual operations, will benefit from additional robust compliance features,” says Russ King, President of MethodSense.

For additional information, please contact Russ King at, 919.607-4775 or via LuminLogic.

MethodSense, a medical device and combination product consulting firm, works with manufacturers, inventors and investors around the world to bring products to market and achieve business success in the U.S., E.U., Canada and other markets. Unmatched regulatory expertise and our purpose-built LuminLogic eQMS and product management software platform uniquely position MethodSense to develop effective strategies for quality compliance and regulatory submissions, from initial filing to product launch and on-going quality and regulatory support. MethodSense has the answers.

Source : MethodSense Follow on Google News


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