Overview

Product video
ComplianceQuest Enterprise Quality Management (EQMS) is an AI-powered, cloud-based solution on Salesforce, offering a fully connected suite that maintains the highest quality standards across the entire product lifecycle. It combines essential modules - Audit Management, CAPA Management, Document Management, Equipment Management, Change Management, Complaints Management, Inspection Management, Nonconformance Management, Supplier Management, Training Management, and Management Review - to ensure that every critical quality function is streamlined and centralized.
Powered by CQ.AI, ComplianceQuest applies predictive analytics to reduce errors, cut costs, and enhance operational efficiency across quality processes. Its intelligent automation capabilities allow proactive quality management and ensure alignment with regulatory standards, including ISO, FDA, OSHA, and EPA. Real-time data insights, role-based dashboards, and automated workflows enable seamless compliance tracking and risk management.
Built for scalability and accessibility, ComplianceQuest EQMS supports mobile access and multilingual needs, making it ideal for both local and global teams. This user-friendly platform replaces disconnected, paper-based systems with a unified digital environment, fostering continuous improvement and enabling seamless collaboration across all departments and sites.
Highlights
- CQ EQMS solution allows a firm to manage quality and product design processes to promote customer, product and supply chain success, reducing risk and provides productivity enhancements gained from sunsetting manual and redundant business processes.
- EQMS Capabilities include: Audit Management, CAPA Management, Document Management, Equipment Management, Change Management, Complaints Management, Inspection Management, Nonconformance Management, Supplier Management, Training Management, Management Review.
- Our EQMS suite monitors the following industry regulations: ISO 9001 ISO 13485, ISO 17025, ISO 27001, AS 9100, IATF 16949, Good Practices (GMP, GxP), ICH Q7-11, 21 CFR Part 11/EU Annex 11 (ERES)