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SYMATESE has always considered the quality of its products and the safety of patients as its main target, and has implemented an effective quality system validated by competent authorities (ANVISA, pharmaceutical agencies) and ISO 13485 and ISO 9001 certifications.

Our daily goal is to guarantee that patients receive a safe, high quality product meeting regulatory and legal requirements.

Every day, in all our activities, we are committed to moving towards excellence and performance.

The integration of tools such as the PDCA (Plan Do Check Act) system and the importance of training in the SYMATESE quality management system contribute to this commitment and guarantee the high quality and safety of our products.

Good Manufacturing Practices (GMP, Quality System Regulation CFR820) and European directive MDD93/42 constitute the regulatory basis of the SYMATESE quality management system.

All our products are CE marked.