Built by someone who understands medical device safety.
Data Intelligence was created to help medical device professionals analyze safety and regulatory data faster, uncover meaningful trends, and reduce the manual effort required to support quality, regulatory, and risk decisions.
From public FDA data to actionable intelligence
Watch this brief overview to see how Intelli-Data helps quality, regulatory, engineering, and risk teams explore complex medical device information.
Turning complex FDA data into usable intelligence
I am a quality professional with more than 25 years of experience supporting product quality systems, risk management, and continuous improvement initiatives. Throughout my career, I have developed a passion for improving efficiency through data analysis, automation, and practical problem-solving.
As regulatory expectations continue to evolve, teams are being asked to analyze larger datasets, identify trends faster, and generate stronger evidence to support quality, safety, and regulatory decisions — often without additional resources.
Data Intelligence was created to address that challenge by transforming publicly available safety and regulatory data into cleaner, normalized, easier-to-analyze information that supports faster and more informed decision-making.
What began as a personal efficiency tool quickly evolved into something larger. The same challenges I was facing exist across quality, engineering, regulatory, and risk management teams throughout the industry.
We started with FDA data because of the rich public datasets available. Additional sources will continue to be incorporated, along with more cleaning, normalization, and cross-dataset analysis options.
Help teams spend less time searching and more time deciding
Data Intelligence helps medical device professionals reduce manual research, identify meaningful safety and regulatory trends, and make better-informed decisions from complex public data.
Combine industry experience with AI-assisted workflows
We combine medical device quality experience, AI-assisted analysis, and normalized data structures to create faster, more reliable, and more meaningful insights for quality, regulatory, engineering, and risk teams.
Questions, feedback, or partnership opportunities?
We would love to hear from medical device professionals, quality leaders, regulatory teams, and organizations interested in better FDA intelligence.
Designed by someone who has worked directly in quality, risk management, and medical device safety.
Data Intelligence was built for professionals who need faster access to meaningful FDA safety, recall, and clearance insights.