Verifarma T&T

17 reviews

Verifarma T&T Cloud is a global leader in the Pharma Serialization and Track & Trace space. With more than 2000 customers worldwide, we cover most serialization regulations around the globe.

Verifarma QMS

0 reviews

Verifarma QMS is a comprehensive cloud-based Quality Management System tailored for the pharmaceutical industry, designed to ensure product quality and patient safety. It centralizes quality assurance and control activities, facilitating compliance with Good Manufacturing Practices (GMP) and international regulations. Key Features and Functionality: - Document Management System (DMS): Enables document request generation, online collaboration, version control, controlled copies, and integrates with Office 365. - Training Management: Maintains individual digital training records, offers online training access, and includes a scoring system with alert notifications. - CAPA and Deviations Management: Facilitates the generation, investigation, task planning, and closure of Corrective and Preventive Actions (CAPA) and deviations, supported by an alert system. - Quality Complaints Handling: Manages complaint generation, evaluation, and integrates with deviations and CAPA processes, ensuring comprehensive quality oversight. - Program Management: Allows for the creation, planning, task assignment, and digital storage of deliverables, with integrated alert systems. - Audits: Supports audit planning, team creation, customized checklists, result evaluation, and tracking of findings with task assignments. - Change Controls: Manages change request generation, collaborative analysis, impact assessment, and task tracking associated with changes. Primary Value and User Solutions: Verifarma QMS enhances operational efficiency by reducing document search and retrieval times, ensuring data integrity through adherence to ALCOA principles, and providing full traceability of changes without data loss. Its cloud-based infrastructure offers secure digital documentation storage, aligning with international standards and certifications such as GS1, ISO 9001, and ISO 27001. By integrating various quality management processes into a unified platform, it empowers pharmaceutical companies to maintain high-quality standards, comply with regulatory requirements, and ultimately safeguard patient health.