Discus QMS - 2026 Pricing, Features, Reviews & Alternatives

Achieve Paperless Quality Excellence with Discus PharmaSuite QMS

Discus PharmaSuite qms empowers pharmaceutical companies to transition to a paperless quality management process while maintaining strict compliance with regulatory standards. By streamlining and automating tasks, our qms enhances operational efficiency and ensures your firm meets industry requirements with ease.

Unified Quality Management Under One Roof

Bring all your quality processes together in a single, integrated platform for better analysis, process improvement, and decision-making. Discus PharmaSuite qms is fully compliant with CFR 21 part 11, as validated by usfda and European regulatory auditors, among others, making it the trusted choice for quality excellence.

Streamlined Quality Management Tailored for Pharmaceuticals

Unlock the full potential of your quality management with Discus PharmaSuite qms. Designed specifically for the pharmaceutical industry, our adaptable, pre-configured workflows seamlessly integrate with your existing systems. The workflow-based system efficiently routes quality events—such as capa, deviations, change control, customer complaints, out of specification (oos), and out of trend (oot) events—through the appropriate departments and stakeholders, ensuring strict adherence to defined procedures.

Key Features and Benefits:

Effortless deviation management: Quickly address deviations to minimize their impact on product quality and compliance.

Proactive risk mitigation: Identify and mitigate potential quality risks before they escalate, safeguarding your operations.

Seamless change control: Centralize and coordinate change management across departments, ensuring consistent communication and alignment.

Effective capa management: Streamline the documentation, tracking, and closure of corrective and preventive actions, driving continuous improvement.

Comprehensive audit trails: Maintain detailed records of all quality activities with extensive audit trails and user authentication for audit readiness and compliance.

Real-time insights: Access live dashboards for real-time visibility into your quality processes, enabling informed decision-making.

Integrated supplier quality control: Ensure high-quality standards throughout your supply chain with robust supplier management tools.

Enhanced document management: Organize and control all quality-related documents in one central location, making them easily accessible and manageable.

Streamlined lab investigations: Conduct thorough and efficient lab investigations to uphold quality assurance standards.

Comprehensive complaint management: Handle customer complaints with a structured, compliant approach, ensuring timely and effective resolutions.

CFR 21 part 11 compliance: Meet stringent fda regulatory requirements for electronic records and data integrity with built-in compliance features.