Usability Documentation Review
Reviewing the usability documentation is important to ensure that Pharma, Diagnostics and MedTech companies comply with regulatory requirements.
Is the Use-Related Risk Analysis (URRA) lacking required information? Are there gaps in the task analysis of a medical device? Is the formative study report missing? These are examples of the shortcomings that a usability documentation review can reveal.
With years of experience solving real-world problems for clients, the usability engineers at MGS Design & Development can help your organization get compliant through a thorough usability documentation review.
