July 13, 2020
July 13, 2020
In the growing and crowded medical software solution market, it is becoming more and more difficult to judge who is capable of providing medical solutions that deliver exceptional value and quality while not compromising on attributes that offer trust. It is hard to judge the book by its cover, and this is also the reason we are relentlessly investing efforts to provide independent assessments of processes used to deliver our solutions and services.
Parsek just reached another significant milestone on the journey to excellence. In June 2020, external auditors confirmed that processes used in the delivery of medical-grade software solutions consistently meet applicable regulatory requirements and use best industry practices as demanded by the ISO 13485:2016 standard.
With this vital piece of the puzzle added into the big picture of Parsek’s quality management, connected to past certification and standardisation, there are no doubts that Parsek is fit for a successful implementation of medical solutions and provisioning of medical devices under MDD and MDR legislative frameworks.
We are fully committed to pursuing the quality mindset by using best practices and ISO recommendations in our daily work further-on!
Read more about our commitment to quality HERE.