Webinar Overview
Look forward to exciting topics, lots of input and inspirations for more efficient work.
Post-market Surveillance (PMS) is one of the most complex processes in medical device quality management systems due to its interface to many other processes. Get more Information in this TechTalk.
Software used for the support of processes in quality management systems (QMS) must be validated to confirm that the software fulfills the intended purpose. Important to understand is, that the validation must be conducted on the basis of the application process and in the IT environment of the software operator.
In this on-demand webinar we will explain the interfaces and demonstrate, how you can link information between these processes in Polarion in order to demonstrate compliance with regulatory requirements.