Ready, set... Get to market!
When you develop life-impacting medical devices, you want to rapidly traverse the course to obtain, and maintain ISO 13485. Scilife can help you gain full compliance, and ensure inspection readiness to get your product to market as fast as possible. We also have modules that can help you streamline your processes, throughout the lifecycle, from initial design to happy patient 🪂 Discover more at: [ Ссылка ]
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We’re here to support Life Science companies to improve quality management, processes, and product development through our pre-validated, and entirely cloud-based SaaS platform: Scilife.
Our vision? To boost science and be the best Life Sciences allies there can be. We help companies ace audits, improve all processes (not just quality-related ones) and save time in the journey toward competitivity in the space.
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Scilife for Medical Devices Companies
Теги
Quality by DesignQuality managementQMSWorkflow automationFDA 21 CFR part 11CAPAs
Document controlChange controlQuality AssuranceRisk AssessmentValidationRegulatory affais and complianceAuditHealthcareLife SciencesDigital transformationCRO laboratoriesGood Laboratory PracticesGMPGAMP 5Medical Devicescloud-based SaaS