July 24, 2017
We are busy bees this summer, and we will be releasing the next version of our KronoDesk help desk system (v2.1) in the next month. In this article we describe the two main new features in KronoDesk 2.1 and what you can expect from the new version.
Read MoreSeptember 18, 2015
When developing software, systems and hardware for use in medical devices, healthcare IT systems or pharmaceutical processes, you need to follow a requirements and quality management process that complies with the FDA Title 21 CFR Part 11 set of Federal Regulations. Part 11 (as it's more commonly called) defines the criteria under which electronic records and electronic
signatures are considered trustworthy, reliable, and equivalent to paper
records.
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