Discus QMS
Who Is the Company Behind Discus QMS?
- Seller: Discus Business Solutions
- Year Founded: 2009
- HQ Location: Ahmedabad, Gujarat
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Twitter: @DiscusSolutions
4 Twitter followers -
LinkedIn® Page: www.linkedin.com
63 employees on LinkedIn®
Total Products under this Category: 389
Last updated: September 01, 2026
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Highlighted products: MasterControl Quality Management System, Qualio, Redzone, EASE, Octave Reliance (ETQ Reliance), SAP Cloud ERP (SAP S/4HANA Cloud), QT9 QMS, and Ideagen Quality Management.
Underlying data: [Grid® JSON](https://www.g2.com/categories/quality-management-qms/grids.json?focus%5B%5D=mastercontrol-quality-management-system&focus%5B%5D=qualio&focus%5B%5D=qad-redzone&focus%5B%5D=ease-inc-ease&focus%5B%5D=octave-reliance-etq-reliance&focus%5B%5D=sap-cloud-erp-sap-s-4hana-cloud&focus%5B%5D=qt9-qms&focus%5B%5D=ideagen-quality-management)
docxpert.io is a cloud-based QM compliance platform designed to run ISO-ready quality systems with less manual overhead. Pricing stays flexible: pay-as-you-go plans start at €89/month with unlimited users/admins. At its core, docxpert.io delivers document control and approvals: lifecycle statuses, versioning with compare and revision cycles, role-based access control, and configurable multi-stage workflows. AI features accelerate authoring and quality by generating documents via a guided wizard, classifying content, running ISO compliance checks, and powering a QM Knowledge Assistant (RAG) to find and summarize the right information fast. Beyond documents, docxpert.io connects the full compliance loop: requirement coverage and automated gap analysis, CAPA with RCA (5-Why/Ishikawa) and effectiveness checks, and training with quizzes and certificates that can be externally verified. Every action is recorded in an immutable audit trail, with optional blockchain stamping and verification URLs for critical events. Supported standards: ISO 9001:2015, ISO 13485:2016, IATF 16949, ISO 14001, ISO 27001. Languages Supported (UI): German (DE), English (EN) docxpert.io combines ISO-focused document control with AI-powered compliance automation and audit-grade evidence in one platform. Unlike generic DMS tools, it’s built around how compliance teams actually work: controlled lifecycles, multi-stage approvals, revision cycles, and a requirement-to-document coverage model that makes gaps visible and actionable. What makes it different is the end-to-end traceability: gap analysis and coverage dashboards, CAPA with structured RCA and validation, training with certificates and verification, and an immutable audit trail with optional blockchain stamping for high-integrity proof. For multi-site organizations, branch & merge and impact analysis help manage local variants while keeping a single source of truth.
Efficient QMS Complete is simple to use, cost effective, cloud-based, paperless management software that simplifies creation, editing and control of documented information for any Company.
Enzyme QMS is 21 CFR Part 11 compliant, validated out-of-box, and offers an industry-leading number of integrations so you can keep using the tools you love. Designed to scale as you scale, Enzyme supports the full product lifecycle, making it the only QMS you’ll ever need. - Complete: Enzyme QMS has everything you need, premarket to postmarket, startup to IPO. - Versatile: Enzyme adapts to your way of working, not the other way around. - Proactive: Our QMS software is continuously evolving to better meet your needs. - Intuitive: Designed by quality & regulatory professionals, for quality & regulatory professionals. Headquartered in South San Francisco, Enzyme was founded in 2017 by industry veterans frustrated by existing QMS solutions. Leveraging our deep experience in regulated software development, we’ve applied the best practices in software system integration to designing a product for all life science companies, including drug, biologic, device, and digital.