The digital solution that ensures traceability and quality in the Life Sciences industry.
Centralize processes, ensure traceability, and comply with regulatory requirements by implementing our Track and Trace, QMS, LIMS, RIMS and Pharmacovigilance solutions.
Pharmaceutical industry trust
More than 2,000 companies trust Verifarma to ensure patient safety.


















Our numbers o Key figures
Managing quality, traceability and regulatory compliance shouldn't be complex or fragmented.


The pharmaceutical industry needs technology that meets its level of regulatory requirement.

Discover our Life Sciences Quality Suite
At Verifarma, we develop comprehensive technological solutions for life sciences and healthcare, accompanying organizations throughout the drug lifecycle: from quality and regulatory compliance, to traceability and business management.
Track & Trace

LIMS
Laboratory Management System

RIMS
Regulatory Affairs System

Pharmacovigilance
Pharmacovigilance Management System




CAPA and deviation management in QMS: from logging to intelligent analysis

The advancement of traceability regulations in the world
Verifarma supports the pharmaceutical industry by ensuring traceability in more than 27 countries, adapting to local regulations and global regulatory compliance.



























Reviews from our customers

“A good option for SMEs. Web-based system. Customizable solutions. Staff flexibility (KAM, PM). Good solution for smaller companies.”

“The solutions are easy to use and any problem is solved quickly, we had a good experience with Verifarma.”

“The best solution for product traceability. A comprehensive system for the administration and control of the traceability of the drugs we handle. And it has a highly qualified team to provide solutions tailored to each business.”
Frequently Asked Questions
Answers to the most common questions about our solutions.
Verifarma specializes in the development and implementation of technological solutions for the pharmaceutical and life sciences industries, focusing on quality management, drug serialization and traceability, and business management. Through its platforms—such as Verifarma Integrated Solutions (QMS, LIMS, RIMS, among others), Track & Trace, and SAP Business One—it helps companies optimize their processes, ensure regulatory compliance, and protect patient safety.
Verifarma Track & Trace is a drug serialization and traceability solution that allows laboratories and players in the pharmaceutical chain to comply with international regulations, such as EU FMD and other global regulatory frameworks. The platform manages the unique identification of products at the unit level and their aggregation at different packaging levels, providing complete visibility and control throughout the supply chain. It operates on a scalable architecture at levels 3, 4 and 5, integrating with line systems, logistics operations and regulatory repositories. In this way, it ensures data integrity, end-to-end traceability and operational efficiency in serialization processes.
Verifarma Integrated Solutions is a modular platform designed to digitize and optimize key processes in the pharmaceutical and life sciences industries. It integrates solutions such as QMS, LIMS, RIMS, pharmacovigilance and document management in a single environment, allowing for centralized, efficient and traceable information management. The platform is aimed at ensuring regulatory compliance, improving the quality of processes and increasing operational efficiency, providing organizations with greater control, visibility and decision-making capacity in highly regulated environments.
Verifarma's Pharmaceutical Quality Suite comprehensively covers the main areas of the quality management system in the pharmaceutical and life sciences industries. It includes features for Quality Assurance (QMS), Quality Control (LIMS), Regulatory Affairs (RIMS), Pharmacovigilance, Document Management (DMS) and Training Management. This coverage allows you to centralize critical processes, improve information traceability, ensure regulatory compliance and promote continuous improvement, providing organizations with a unified and efficient view of their quality operations.
Verifarma has global implementations in more than 26 countries, supporting pharmaceutical and life sciences companies in different markets with solutions adapted to local and international regulatory requirements. Its international presence allows it to offer extensive experience in regulations such as EU FMD, FDA, ANMAT, INVIMA, among others, providing support and specialized knowledge in each region where it operates.
Verifarma has international certifications ISO 9001 and ISO 27001, which guarantee high standards in quality management and information security. In addition, it is one of the first companies certified by EMVO, complying with GS1 standards since 2008 and with the requirements of FDA 21 CFR Part 11 through validatable software under GAMP 5 guidelines. In addition, its solutions are designed to comply with EU Annex 11, ensuring their suitability to highly regulated environments.
Yes, Verifarma offers 24/7 customer support in English and Spanish, ensuring continuous and efficient service in all the markets where it operates. In addition, through its Customer Success program, it actively accompanies its customers to maximize the value of the solution, ensure operational continuity and promote continuous improvement of their processes.
Request a demo
Learn how our solutions can adapt to your processes and regulatory requirements. Our team will accompany you for a personalized demonstration.














