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The secret to ensuring quality in an FDA 510k medical device submission

One of the most important documents for an FDA 510k medical device submission is the anomalies document, which outlines what bugs exist in the product and what risks it presents to patient safety. When the entire goal of your product is to improve patient outcomes,...

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How to approach requirements gathering for legacy system rewrites

One of the first major hurdles to legacy system modernization is requirements gathering: New requirements should be accurately written and detailed. They may introduce deliberate changes, but shouldn’t overlook the intricacies of how the current system operates. This...

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Email Refactoring: Making Communication as Clean as Code

Effective CommunicationEarly in developer careers, there’s a natural emphasis on writing clean code and becoming a technical expert. Great developers take that same passion for communicating in code, and strive to improve their communication with non-technical...

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Latest Post

blog

The secret to ensuring quality in an FDA 510k medical device submission

blog

How to approach requirements gathering for legacy system rewrites

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Email Refactoring: Making Communication as Clean as Code

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