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Company description

Verifarma develops digital solutions for pharmaceutical traceability and quality management, serving the life sciences and healthcare industries. The company offers a suite of validated software platforms covering Track & Trace, Quality Management (QMS), Laboratory Information Management (LIMS), Regulatory Information Management (RIMS), and Pharmacovigilance, designed to help organizations manage the full lifecycle of a medicinal product while meeting local and international regulatory requirements.

Founded over 16 years ago, Verifarma serves more than 2,000 customers — including laboratories, distributors, wholesalers, and pharmacies — across 27 countries. The company holds ISO 9001 and ISO 27001 certifications, aligns with GAMP 5 guidelines for validatable software, complies with GS1 standards, and meets FDA 21 CFR Part 11 and EU Annex 11 requirements. Technical support is available 24/7 in three languages, and the company reports a 98% customer satisfaction rate.

Core Product Suite

  • Track & Trace (Serialization & Traceability): Provides unit-level traceability of medicines across the entire supply chain, supporting compliance with local and international serialization regulations.
  • QMS (Quality Management System): Manages deviations, CAPAs, audits, complaints, change control, and quality programs within a single validated platform.
  • LIMS (Laboratory Management System): Digitalizes assays, samples, results, and reports, ensuring data integrity and complete traceability within laboratory environments.
  • RIMS (Regulatory Affairs System): Centralizes the management of regulatory registrations, submissions, and deadlines in a controlled environment.
  • Pharmacovigilance System: Digitalizes and centralizes pharmacovigilance management through a validated, secure platform adapted to international regulations, supporting data integrity, patient safety, and auditable collaborative processes.
  • SAP Business One (Argentina only): An ERP solution adapted to the pharmaceutical sector for optimizing operational management and traceability.

AI Capability

  • Verifarma offers an AI assistant called Vera, integrated into its quality solutions. Vera is designed to simplify access to information, optimize processes, and support decision-making within regulated quality workflows.

Global Traceability Coverage

  • Verifarma supports pharmaceutical traceability compliance across more than 27 countries, adapting to varying local regulatory frameworks.
  • Countries with active implementations or regulatory coverage include Argentina, the United States, the European Union, Turkey, Russia, China, India, South Korea, Saudi Arabia, the United Arab Emirates, Canada, Kazakhstan, Uzbekistan, and others.
  • The company also provides a practical implementation guide for regulatory bodies evaluating the introduction of drug serialization and traceability legislation, covering key points for compliance with local requirements and international standards.

Compliance and Certifications

  • ISO 9001 certified for quality management and ISO 27001 certified for information security.
  • Software developed in accordance with GAMP 5 guidelines, making it suitable for validated use in regulated environments.
  • Compliant with GS1 standards since 2008, FDA 21 CFR Part 11 for electronic records and digital signatures, and EU Annex 11 for computerized systems.

Deployment and Support

  • Solutions are web-based and described as customizable, with flexibility suited to organizations of varying sizes including SMEs.
  • The company provides 24/7 technical support in three languages, covering implementation, operation, and post-sales stages.
  • Verifarma offers 13 specialized solutions designed to cover the principal processes of the pharmaceutical sector.

Customer references include Polisano Pharmaceuticals, Globalfarm S.A., and quality assurance professionals from serialization roles, who cite ease of use, rapid issue resolution, and the availability of tailored support as notable aspects of working with Verifarma.

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