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.

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Simpler and more controlled audits
International regulatory compliance
Process efficiency

Pharmaceutical industry trust

More than 2,000 companies trust Verifarma to ensure patient safety.

ISO 9001/ISO 27001
Quality and safety management.
GAMP 5
Validated software
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GS1
Meeting standards since 2008
FDA Certified Compliance seal.
FDA 21 CFR Part 11
FDA compliance and digital signatures
Blue circular badge with text EU COMPLIANT and Annex 11.
EU ANNEX 11
Compliance with EU guidelines
Reliable, validated technology for regulated and demanding environments.

Our numbers o Key figures

16
Years of industry experience
Proven experience in developing solutions for regulated environments.
+2000
Companies trust our solutions
Laboratories, distributors, drugstores and pharmacies that use our platforms on a daily basis.
27
Countries where Verifarma operates
Active implementations in markets with different regulatory frameworks.
13
Solutions designed for the industry
Specialized tools that cover the main processes in the sector.
24/7
Technical support in 3 languages
Continuous support during implementation, operation and post-sales.
98%
Customer satisfaction rate
Long-term relationships based on trust and results.

Managing quality, traceability and regulatory compliance shouldn't be complex or fragmented.

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

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Our Solutions

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

Serialization & Traceability
Ensure the unit-level traceability of drugs throughout the supply chain, complying with local and international regulations.
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LIMS

Laboratory Management System

Digitize tests, samples, results and reports, ensuring data integrity and full traceability.
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RIMS

Regulatory Affairs System

Manage regulatory records, filings, and deadlines in a centralized and controlled manner.
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Pharmacovigilance

Pharmacovigilance Management System

Digitize and centralize your pharmacovigilance management with a validated, secure solution that complies with international regulations. Ensure data integrity and patient safety with collaborative and auditable processes.
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Our AI solution
Vera, AI applied to quality
An intelligent assistant integrated into our quality solutions, designed to simplify access to information, optimize processes and support decision-making.
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SAP Business One

Exclusive to Argentina
ERP tailored to the pharmaceutical sector to optimize management and operational traceability.
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CAPA and deviation management in QMS: from logging to intelligent analysis

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Global traceability

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.

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DEADLINE
Expected
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Reviews from our customers

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

Péter Dombai
Serialization Manager, Quality Assurance

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

Carmen Dobrea
Production Manager,
Polisano Pharmaceuticals

“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.”

Ricardo Barriopedro
Systems Manager,
Globalfarm S.A.
The opinion of our customers supports us
Success stories tested.
Real experiences of our customers.

Frequently Asked Questions

Answers to the most common questions about our solutions.

What does Verifarma specialize in?

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.

What is Verifarma Track & Trace?

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.

What is Verifarma Integrated Solutions?

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.

What areas does Verifarma's Pharmaceutical Quality Suite cover?

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.

In how many countries does Verifarma have implementations?

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.

What certifications does Verifarma hold?

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.

Does Verifarma offer customer support?

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.

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