HOW WE DO IT
Neolife operates under a rigorous Quality Management System and abides to all Portuguese health regulations. We only distribute high-quality certified products with proven international safety and efficacy. All products we distribute are CE-marked and comply with all applicable Portuguese regulations.
Additionally, Neolife maintains a robust Cybersecurity Management System designed to protect sensitive data, ensure the integrity of digital processes, and safeguard confidential information across its operations. Our cybersecurity framework is aligned with internationally recognized best practices, ensuring secure data handling, risk mitigation, system resilience, and continuous monitoring to prevent unauthorized access, breaches, or operational disruptions.
QUALITY:
Because quality can, and must, be auditable, Neolife takes pride in its ISO 13485 certification for excellence in Medical Devices.
Certification in accordance with ISO 13485 recognizes that an organization has the ability to provide medical devices and related services that consistently meet customer requirements and applicable regulatory requirements.
Organizations may be involved in one or more stages of the life cycle, including design and development, production, storage and distribution, installation, or servicing of a medical device, as well as the design and development or provision of associated activities (for example, technical support).