Quality Policy

BioPorto is committed to the highest level of quality in the manufacture, sale and support of its products. Quality and compliance with all applicable regulatory requirements and customer satisfaction must underlie the company's efforts in manufacturing, advertising, sales, shipping and technical support.

BioPorto is committed to effectively implementing and continuously improving its quality management system in accordance with the European IVD directive, the Canadian medical device regulations and ISO 13485 requirements.BioPorto is ISO 13485:2016 certified and holds an MDSAP Certificate. 

BioPorto aims to please the customers while paying due regard to the interests of the company's stakeholders.

Updated April 2nd 2019


                  ISO 13485 

                 ISO 13485 MDSAP