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
These Terms and Conditions (“Terms") governing the sale of products and related services ("Products”) from BioPorto Diagnostics A/S ("BIOPORTO") and Buyer. Any deviating conditions or reservations by Buyer shall only be binding if confirmed in writing by BIOPORTO. Conditions are also applicable in individual cases where Terms are not attached, but which Buyer has been made aware of the Terms.