Verifarma delivers an integrated suite of validated software solutions for the life‑science and pharmaceutical sectors, covering quality management (QMS), laboratory information (LIMS), risk management (RIMS), and global track‑and‑trace serialization. The platform ensures compliance with regulations such as FDA 21 CFR Part 11, EU Annex 11, and GS1 standards across more than 27 countries, helping companies protect patient safety and streamline audit readiness. Its solutions also integrate with ERP systems like SAP Business One to support end‑to‑end business operations.
Funding
Funding not disclosed
Founders
Product
Problem
Pharmaceutical and life‑science companies must manage complex quality, regulatory, and traceability requirements across multiple jurisdictions, often using disparate systems that hinder data consistency and audit readiness.
Solution
Verifarma offers an integrated suite of validated software modules—including Track & Trace, Quality Management System (QMS), Laboratory Information Management System (LIMS), Regulatory Information Management System (RIMS), and pharmacovigilance tools—to centralize these processes. The platforms support global serialization and end‑to‑end drug traceability in over 27 countries, adapting to local regulations such as FDA 21 CFR Part 11, EU Annex 11, GAMP 5, and ISO 9001/27001. By providing multilingual, 24/7 technical support and a validated, scalable architecture, Verifarma enables organizations to maintain compliance, protect patient safety, and streamline operations throughout the drug lifecycle.
Target Audience
Primary customers are pharmaceutical manufacturers, contract labs, distributors, and pharmacy chains that require integrated quality, compliance, and traceability solutions across regulated markets.
Features
- Track & Trace module with unit‑level serialization, aggregation, and real‑time visibility across the supply chain
- QMS solution delivering electronic document control, audit trails, and digital signatures compliant with FDA 21 CFR Part 11 and EU Annex 11
- LIMS for laboratory data capture, workflow automation, and integration with analytical instruments
- RIMS for managing regulatory submissions, product registrations, and compliance documentation
- Pharmacovigilance platform supporting adverse event reporting and safety signal management
- Validated, GS1‑compatible architecture with support for ISO 9001, ISO 27001, and GAMP 5 standards
- Multilingual interface and 24/7 support in three languages to accommodate global operations