Comprehensive solution for managing the pharmacovigilance area.
Digitize and centralize pharmacovigilance management with a validated, secure solution that complies with international regulations. Ensure data integrity and patient safety with collaborative and auditable processes.
Benefits of the Pharmacovigilance System
Verifarma FVG is a comprehensive pharmacovigilance management solution designed specifically for the pharmaceutical industry. It allows for the centralized recording, monitoring, and analysis of adverse events, ensuring data traceability, regulatory compliance, and patient protection. Its collaborative approach connects all stakeholders in the process—from report reception to final validation—in a secure and validateable environment compliant with GAMP 5, ISO 9001, and ISO 27001 guidelines.
Multidisciplinary Collaboration
It facilitates joint work between pharmacovigilance, quality and regulatory issues, centralizing information and case monitoring.
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Secure Registration and Tracking
It allows a complete and traceable record of each adverse event, with detailed action tracking and automatic auditing.
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Validable System
Complies with international validation standards to ensure system reliability and data integrity.
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Integrated Document Management
It centralizes all the documentation of the regulatory process and facilitates access to reports, reports and updates.
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.
