Persyst Quality Policy

The policy of Persyst Development Corporation is to strive for the highest standard of quality in our operations and to continually endeavor to satisfy the expectations of our customers with respect to all the products and services we offer. Persyst is committed to comply with quality requirements, to continually review and improve the effectiveness of the quality management system and its suitability.

Certificate, EN ISO 13485:2016
Medical devices – Quality management systems –
Requirements for regulatory purposes
(ISO 13485:2016)
DIN EN ISO 13485:2016

Certificate, ISO 13485:2016 (MDSAP)
Australia TGA, Health Canada, USA FDA, MHLW / PMDA

Persyst Development Corporation has implemented a Quality Management System in accordance with:

ISO 13485:2016
Medical Devices-Quality Management Systems-Requirements for regulatory purposes