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Life Science

Welcoming Jamie Moss and Glenn Abood to Verifarma’s Board of Directors

Verifarma Announces New Board of Directors with Jamie Moss and Glenn Abood

Margarita Ramos Otero

Content Creator

QMS para la industria farmacéutica: cómo demostrar control de calidad ante auditorías regulatorias

Descubrí cómo un eQMS integrado permite a las empresas farmacéuticas de Life Sciences gestionar desviaciones, CAPAs y auditorías con trazabilidad completa y preparación regulatoria continua.

Margarita Ramos Otero

Content Creator

Pharmaceutical Serialization in Europe 2026: Moving Beyond FMD Compliance

Pharmaceutical Serialization in Europe 2026: Beyond FMD Compliance

Margarita Ramos Otero

Content Creator

Verifarma participó por primera vez en ExpoFarma México 2026 y fortaleció su presencia en la industria farmacéutica de la región

Margarita Ramos Otero

Content Creator

Data Integrity en laboratorios farmacéuticos: por qué el LIMS ya no es opcional

Margarita Ramos Otero

Content Creator

RIMS en Latinoamérica: por qué la gestión regulatoria ya no puede depender de procesos manuales

Margarita Ramos Otero

Content Creator

Auditorías híbridas en Life Sciences: el rol clave del QMS digital en la preparación regulatoria

Auditorías híbridas en Life Sciences: el rol clave del QMS digital en la preparación regulatoria

Margarita Ramos Otero

Content Creator

Verifarma announces its strategic partnership with MTIP to accelerate its global expansion in pharmaceutical technology.

Verifarma announces a strategic partnership with MTIP to accelerate its global growth, enhance its traceability platform, and expand its quality management (eQMS) solutions.

Francisco Porzio

Content & Communication Lead | Verifarma

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

Discover how QMS software can automate the management of pharmaceutical CAPAs and quality deviations, detecting patterns and preventing recurrences through intelligent analysis.

Francisco Porzio

Content & Communication Lead | Verifarma

Preparing for an audit: good practices and digital tools

Discover how a quality management system (QMS) helps laboratories document, prevent errors and pass FDA, EMA or ANMAT audits with digital evidence and full traceability.

Francisco Porzio

Content & Communication Lead | Verifarma

How to Implement a National Drug Traceability System: A Guide for Regulatory Entities

Guide for regulatory entities on how to implement a national drug traceability system, based on GS1 standards and international models.

Francisco Porzio

Content & Communication Lead | Verifarma

Validated quality management systems and artificial intelligence: the future in regulated environments

QMS with artificial intelligence: the future of quality management in regulated industries

Margarita Ramos Otero

Content Creator