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CORE QHSE CAPABILITIES
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Document management & version control
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Training management
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Incident/notification management
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Audit scheduling & execution
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Risk management
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Custom forms & templates
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Analytics & reporting
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ISO 9001 compliance support
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ISO 27001 compliance support
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LIFE SCIENCE DIFFERENTIATORS
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Used by 700+ life science companies
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GxP, ISO 13485, FDA & EMA requirements
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Change control for validated processes
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(version control only)
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21 CFR Part 11-compliant e-signatures
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Post-market surveillance and pharmacovigilance
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Supplier qualification for life sciences
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Life science validation documentation
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Life sciences document templates & workflows (CAPAs, deviations, NCRs vs. generic incidents)
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AI compliance gap analysis
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Expert life science regulatory support
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PLATFORM QUALITY
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Native document editing & collaboration
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Limited
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Comprehensive integration suite
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API available
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Ranked easiest eQMS to use (G2)
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Ranked strongest customer support (G2)
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BEST FOR
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Life science logistics suppliers |
Only internal QHSE
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