Nymi has implemented a Quality Management System (QMS) that aligns with our customer requirements and guides the development of products and solutions in compliance with GAMP5 (Good Automated Manufacturing Practice) guidelines by looking at the pharmaceutical manufacturing process as a whole.

Nymi develops products and solutions with high traceability to ensure data integrity and security is maintained throughout the pharmaceutical manufacturing lifecycle.

To support our customer needs, we tailor our solutions to enable seamless integration and a structured qualification and validation approach which is in line with regulatory requirements and the GAMP5 recommendations.

Additional documentation and guides are provided to support implementation and system validation into GMP (Good Manufacturing Practice) environments to ensure pharmaceutical products are consistently produced, according to defined quality standards, every single time.