Quality Management System (QMS) software designed for life sciences and pharmaceutical organizations to manage compliance, documentation, and GMP-ready processes. Automates quality workflows from research through manufacturing scale-up, enabling streamlined regulatory compliance and process control ...
Manufactured by
Scilife NV
Ixelles (Brussels), Belgium
Because when we all embrace quality, brilliant things happen! At Scilife, we help people and companies transform quality into a catalyst for value creation, making Smart Quality a culture and infusing it throughout the entire organization. This recasts quality as a competitive advantage instead of a simple regulatory requirement. But, what embeds quality into a company s culture? And how, exactly, does an organization benefit as a result? These questions are at the core of Scilife. The Scilife Smart Quality Platform brings clarity to quality and compliance by combining powerful quality management tools with advanced data analytics, augmented learning, and gamification. Hundreds of leading life sciences companies worldwide like Novartis, Biocartis, Yusen Logistics, Polpharma, Pendulum, and many more trust Scilife to manage their quality processes, empower employees to take quality ownership, enhance efficiency and transparency, and reduce compliance risk. The impact? Improving patients' lives through safer, more effective healthcare solutions globally.
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Digital Life Sciences GmbH · Germany
GxP-compliant electronic quality management and document management system for regulated life sciences organizations. Enables digital archiving, approval workflows, and electronic signatures per FDA 21 CFR Part 11 and EU-GMP Annex 11 requirements. Supports batch documentation, controlled printing, and full document lifecycle management from creation through retirement.
EDDA Technology,Inc. · China
IQQA®-eQMR is a healthcare IT system designed to streamline quality management and regulatory compliance in medical device and IVD manufacturing. The platform enables organizations to document, track, and manage quality records, corrective actions, and regulatory submissions efficiently. It supports FDA, ISO, and international compliance requirements for medical device manufacturers.
provita medical gmbh & co. kg · Germany
Comprehensive quality management software designed for medical device manufacturers to ensure compliance with regulatory standards and maintain product quality throughout the manufacturing process.
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