Scilife is a validated electronic Quality Management System (eQMS) purpose-built for life sciences organizations, including Pharma, Biotech, and Medical Device companies.
Scilife consolidates the entire quality management lifecycle into a single, compliant platform—covering document control, training management, deviations, CAPAs, change control, audits, supplier and risk management—so quality teams can work efficiently while remaining continuously audit-ready.
Designed for GxP-regulated environments, Scilife enables quality-driven organizations to automate quality processes, reduce manual and repetitive tasks, and gain real-time visibility into what’s open, overdue, and at risk across workflows. The result: fewer surprises during inspections and more time focused on meaningful quality improvement.
＋ What teams achieve with Scilife:
• Reduce operational overhead while strengthening quality governance
• Standardize quality workflows across products, sites, and global teams
• Maintain complete, traceable audit trails for inspections and internal audits
• Prepare smoother regulatory submissions with structured, reliable quality data
Customers report up to 50% lower quality assurance costs and up to 30% faster time-to-market after adopting Scilife.
＋ Built for compliance, without the burden.
Unlike general-purpose QMS or document management tools, Scilife provides a validated, GAMP 5-aligned eQMS software out of the box, significantly reducing validation effort and long-term maintenance.
Automatic updates, built-in validation tools, and controlled releases allow teams to stay compliant with evolving regulations without heavy documentation or revalidation cycles.
Organizations typically deploy Scilife faster than legacy eQMS solutions, while maintaining the level of rigor expected by regulators and notified bodies.
＋ Scalable, flexible, and ready to grow with you.
Scilife’s flexible licensing model and product scalability allow teams to start with what they need today and expand as operations grow—without disrupting compliance or efficiency.
Tiered pricing and rapid onboarding make it easy to adopt Scilife at any stage, from early-stage companies to global, multi-site organizations.
＋ Trusted by regulated teams worldwide
Scilife is trusted by hundreds of life sciences companies worldwide. The platform supports compliance with FDA 21 CFR Part 11, ISO 13485, EU MDR, MDSAP, GxP, and ICH Q10 requirements.
Behind the software is a dedicated customer success team who understand the realities of regulated environments and support teams well beyond onboarding.
＋ Predictable quality—scaled across teams.
Scilife helps life sciences teams move from reactive quality management to proactive, data-driven, and continuously improving quality systems.
Ready to build a brighter, more resilient quality foundation?
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