QA Stack
A modular platform offering eQMS, eBMR, LIMS, and DMS modules for managing deviations, CAPAs, batch records, lab testing, SOPs, and audit trails in pharmaceutical manufacturing.
Launch screenshots from Product Hunt, Jun 2026
A modular quality management platform for pharmaceutical manufacturing that provides electronic Quality Management (eQMS), Batch Records (eBMR), Laboratory Information Management (LIMS), and Document Control (DMS) modules, each deployable standalone. It solves the problem of fragmented, paper-based compliance processes by digitizing deviations, CAPAs, batch records, SOPs, and lab testing into a unified, validation-ready system. Sells to quality assurance, production, and compliance teams at mid-market and enterprise pharmaceutical companies. Positioned as a modular alternative to monolithic suites, allowing customers to buy only the modules they need and connect them as operations grow, with embedded GxP and 21 CFR Part 11 compliance.
Key features
- Automate deviation logs and CAPAs
- Electronic batch records with line clearance
- SOP document control with versioning
- Lab material testing and specs tracking
- Audit trail with electronic signatures
- Change control and risk register
- Supplier and audit management
- Training and qualification tracking
- APQRs, trends, and KPIs analytics
- 21 CFR Part 11 compliant signatures
- LinkedIn<0.1/day
- No GTM activity detected
- Manufacturing industrial
- Enterprises