RIMS | Regulatory Affairs Management System
Centralize and control all regulatory information for your products on a single validated platform. Manage records, renewals and documentation with full traceability and global compliance.
A Regulatory Affairs Management System
Verifarma RIMS is a solution designed to automate, standardize and secure the management of regulatory records and submissions within the pharmaceutical and life sciences industry. The platform allows Regulatory Affairs teams to maintain full traceability of files, documents and critical dates, improving operational efficiency, regulatory compliance and collaboration between areas.
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Complete record management
Manage the full cycle of health records, including registrations, renewals, extensions and extensions, maintaining clear control of each record.
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Regulatory document management
Centralize all regulatory documents on a secure and validated platform, ensuring controlled access and full traceability of information.
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Collaborative work
Facilitate the participation of all areas involved in the regulatory process, such as regulatory issues, quality, production and supply chain.
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Registration and traceability
Record every action and movement within the system, ensuring data integrity and the complete history of each regulatory file.
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.
