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LIFE SCIENCES
Electronic Submissions Review
The Client
A major life sciences regulatory authority in the United States, sought to transform its submission review operations in order to respond more quickly to emerging scientific, technological, and economic trends.​
The Challenge
The organization needed to boost employee productivity and accountability while improving data accuracy and timeliness for better decision-making. Their processes were paper-based, localized, and data was stored in text documents, making information retrieval challenging. Document sharing was inefficient, affecting performance and training.
The Lowcodeminds Solution
Lowcodeminds delivered a low-code digital review application built with Appian that supports 510(k) submissions for medical device authorization. This application integrates with existing systems, modernizing legacy tools and enhancing data quality through automation.​
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