A Quality Management System (QMS) is the cornerstone of compliance and continuous improvement in the life sciences industry. It enables organizations to manage quality processes, documentation, and audits in a structured, traceable, and fully compliant way. In an industry where precision, patient safety, and regulatory expectations are non-negotiable, a modern QMS isn’t just a necessity — it’s a strategic asset.
Regulatory authorities and global markets demand increasing levels of quality assurance, risk control, and traceability. Paper-based systems or legacy tools can’t keep up with the pace of change or the scale of complexity. A modern QMS transforms quality from a regulatory burden into a driver of business excellence.
Ensure readiness for audits and inspections with complete traceability, built-in SOP controls, and automated audit trails.
Unify quality processes like CAPAs, deviations, change controls, and complaints in one integrated system.
Automate repetitive tasks, approvals, and notifications to speed up resolution times and reduce human error.
Track issues, trends, and performance with dashboards and analytics to foster proactive decision-making.
Identify, assess, and mitigate quality risks early with integrated risk management tools.
A cloud-native solution designed for life sciences, offering end-to-end process automation and seamless connectivity with training, documents, and quality events. It enables global teams to work from a unified platform, accelerating issue resolution and ensuring compliance.
A modular and configurable system focused on efficient compliance with GxP requirements. Particularly valued for its strong audit trail management and ease of integration with regulatory processes.
Part of a broader unified platform, CARA allows QMS processes to coexist with regulatory and clinical content in a single environment — delivering unmatched scalability, configurability, and user experience.
Strategic pre-implementation analysis to align the system with your quality goals;
Full system configuration and implementation adapted to your workflows;
Seamless data migration and system integration;
Custom user training to ensure confident use from day one;
Complete system validation aligned with current GxP and ISO standards;
Ongoing support to keep your QMS performing optimally.
eLife Sciences is a team of experts with unique experience in compliance, validation and quality assurance (QA). We provide services to companies in regulated industries with a special focus on life science.
