Digital Quality Management in Pharma
Discover how cloud-first, AI-powered QMS platforms are transforming quality, compliance, and batch release in pharma. IntuitionLabs, based in San Jose, CA, helps organizations modernize with secure, compliant, and scalable quality management solutions.
Why Digital Quality Management Matters in Pharma
The pharma QMS market is forecast to reach $3B by 2030, driven by cloud SaaS, AI, and new FDA/EU regulations. IntuitionLabs can help you digitize CAPA, deviations, audits, and batch release—accelerating compliance and inspection readiness.
- Digitize CAPA, deviations, change control, and audits
- Integrate with LIMS, ERP, MES, and CRM (Veeva, SAP, Salesforce)
- Enable predictive analytics and generative AI for quality events
- Ensure global inspection readiness and electronic validation packs
- Meet FDA 21 CFR Part 11, QMSR, EU Annex 11, ISO 13485, GDPR
What Features Should a Modern QMS Platform Include?
Digitize Quality & Compliance
Modern QMS platforms digitize CAPA, deviations, and audits—reducing manual effort and accelerating compliance.
AI & Predictive Analytics
Leverage generative AI for document translation, deviation summaries, and predictive CAPA analytics.
Integration & Validation
Open APIs and cloud-first SaaS enable seamless integration and electronic validation packs.
Frequently Asked Questions
Ready to modernize your quality management?
Contact IntuitionLabs to discuss how we can help you design and implement a modern, compliant QMS solution.
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