Quality Department

Ocupharm Diagnostics has implemented an integrated management system for Good Laboratory Practices (GLP) and the international standard UNE-EN ISO 9001:2015, under the Scope of:

Management, design, and assistance for the research of ophthalmic products:

The Quality department is responsible for continuously overseeing the proper compliance with GLP and ISO 9001 requirements, based on continuous improvement and aiming to meet legal and customer requirements.

For correct and effective management, the integrated GLP and quality system is 100% computerized. The entire project management process is handled through a single program (Gesiso 9000), from the client’s quote request to the completion of the study, ensuring record traceability and report generation.

Quality, GLP, and environmental policy: