Pharmacolog AB has today received its certificate in accordance with ISO 13485: 2016 (Medical devices - Quality management system - Requirements for regulatory purposes). The certificate is issued by Svensk Certifiering Norden AB and certifies that Pharmacolog AB has a quality management system that meets the requirements regarding development, manufacture, distribution, installation and service of medical technology products. ISO 13485 is an internationally recognized standard that complies with the regulations and regulatory requirements required to provide medical devices and related services in Europe. The standard is well established and internationally accepted.

Mats Högberg, CEO, comments: "The certification of our quality system and the CE marking of our product DrugLog is an important step in ensuring that we have a functioning quality process in the further development of a new generation of medical technology products. Having the regulatory requirements in place and having a quality system that works, which the certificate is proof of, is a prerequisite for us to be able to act in the market. Especially important as we have entered into exciting partnerships and are about to establish new products."