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FDA Logo

FDA Releases Final Guidance on Premarket Submissions for Device Software Functions

By MedTech Intelligence Staff

“Content of Premarket Submissions for Device Software Functions” covers recommended documentation sponsors should include in premarket submissions for FDA’s evaluation of safety and effectiveness of device software functions. The agency is hosting a webinar for industry on July 20 to provide an overview and answer questions about the new final guidance.

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Steve Thompson
Steve Thompson

Risk-Based CSA Validation: Ensuring the Least Burdensome Approach

By Steve Thompson

When it comes to testing, the most significant difference between CSV and CSA is that CSV focuses on a “test everything” approach, while CSA encourages us to use critical thinking to test more effectively. The following article outlines how companies can identify the appropriate degree of testing rigor for risk-based CSA validation to ensure the least burdensome approach.

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Adrian Jennings
Adrian Jennings

Using RTLS To Improve Operational Efficiency

By Adrian Jennings

In leveraging the valuable insights delivered by real-time location systems (RTLS) technology, hospitals and healthcare facilities are able to undergo the kind operational overhaul they so desperately need, boosting ROI while simultaneously allowing for better working conditions for staff as well as more focused, immediate care for patients.

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Binary code
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Automating Computer Systems Validation for Your QMS

By Davor Milosevic, Massimo Franza

Regulatory requirements for computer systems validation (CSV) have long been in place, but their compliance requires considerable time and resources. In the life sciences industry, traditional validation processes add to project timelines and costs, affecting time to market and preventing the deployment of newer versions of software. In addition to improving accuracy and coverage, automated CSV processes can create the same artifacts as manual execution and expedite the upgrade timeline.

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