QMS | Quality Management System for Laboratories
Optimize the quality management of your laboratory with a platform that centralizes diversions, CAPAs, audits and documentation, ensuring traceability, efficiency and regulatory compliance.
Comprehensive optimization of the pharmaceutical quality management system
The Verifarma Integrated Solutions (VIS) QMS module centralizes all quality management processes on a single validated platform. This allows you to obtain full traceability of each process, simplify audits and maintain full control over each stage of the quality cycle.
.svg)
Deviation and Layer Control
Record, investigate and manage quality deviations in a structured way, implementing corrective and preventive actions (CAPA) to ensure continuous improvement of processes.
.svg)
Audit Management
Plan, execute and document internal and external audits from a single platform, making it easier to track findings and prepare for regulatory inspections.
.svg)
Management of Claims and Non-Conformity
Centralize the recording and monitoring of claims and non-compliances, ensuring analysis, resolution and full traceability of each case.
.svg)
Change Control
Manage and document changes to processes, procedures or systems, ensuring impact assessment, approval and traceability.
.svg)
Follow-up of Action Plans
Monitor the progress of corrective and preventive actions, ensuring that deadlines, managers and results are met.
.svg)
International Regulatory Compliance
Ensure compliance with international regulations and standards such as GAMP 5, FDA 21 CFR Part 11, ISO 9001 and ISO 27001, facilitating regulatory audits and validations.
When quality becomes intelligent
Vera joins our product to transform quality data into actionable information, improving efficiency and operational control.
Why choose Verifarma?
With more than 16 years of experience, we support life science in complying with traceability regulations in Latin America, Europe and other markets.
Electronic signature and Audit Trail. Cloud solution with a focus on data integrity. Full traceability of information. Notification and alert system.
21 CFR Part 11 compliance. Validable solution under GAMP 5 — Category 4. Platform ready to adapt to regulatory changes. Specific design for the pharmaceutical industry.
Paperless operation. Agile access to information. Greater speed and efficiency in operational processes.
24/7 technical support. Cross-cutting platform that connects multiple areas of the organization. Remote access from any location. Intuitive and easy to use interface.
Discover our Pharmaceutical Quality Suit
QMS is part of the Pharmaceutical Quality Suite, together with modules that cover all critical areas of the quality system.
Pharmaceutical industry trust
Change the drop for: More than 2000 companies trust Verifarma to ensure patient safety.
Reviews from our customers
“Meiji decided to trust Verifarma to modernize the processes that existed on paper, improve data integrity and facilitate digital and remote work.”
“I am extremely satisfied with Verifarma's document management system. With their help, I can access all my critical documents efficiently and securely from anywhere. I appreciate that they have adapted to my quality system.”
“We have implemented Verfarma Integrated Solutions to improve the efficiency, security and accessibility of our files, optimizing search, storage and collaboration processes, thus ensuring more effective and organized document management”
Request a demo
Learn how our solutions can adapt to your processes and regulatory requirements. Our team will accompany you for a personalized demonstration.
