Ocupharm Diagnostics has implemented a management system integrated by Good Laboratory Practices (GLP) and the international standard UNE-EN ISO 9001:2015, under the Scope of:
MANAGEMENT, DESIGN AND RESEARCH ASSISTANCE FOR PRODUCTS FOR OPHTANMOLOGICAL USE:
- PHYSICAL – CHEMICAL PROPERTIES
- MEASUREMENT METHODS
- PHYSICAL COMPATIBILITY
- CLINICAL RESEARCH
- BIOLOGICAL EVALUATION
The Quality department is responsible for continuously monitoring correct compliance with GLP and the requirements of the ISO 9001 standard based on continuous improvement and aimed at meeting legal and customer requirements.
For correct and efficient management, the integrated GLP and quality system is 100% computerized. Carrying out all project management using a single program (Gesiso 9000), from the client’s request for an offer to the completion of the study, the traceability of records and the generation of reports.