QMS and Regulatories
The QMS – Quality Management System aims to validate all processes required by regulatory bodies’ regulations.
Quality management for the pharmaceutical industry
With our system, you will ensure the constant improvement of your company’s processes, as well as guarantee the quality of your products and services.
Aligned with the guidelines of RDC-301 – Good Manufacturing Practices for Medicines, from the National Health Surveillance Agency (ANVISA), four modules of the Interact Suite SA have been approved in quality management programs of laboratory sector clients in Brazil.
Explore the Quality Management modules
Benefits and features
- Compliance with RDC 301 guidelines – Good Drug Manufacturing Practices, by Anvisa
- Control and alignment of strategic and operational indicators
- Management tools for visual monitoring of indicators
- Control of action plans and projects with schedule and workflow
- Sophisticated management analysis tools
- Integrated management of critical analysis events
The QMS and Regulatory Solution complies with the main guidelines:
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