Driving Innovation: Accelerating Standard Compliant Data Generation through AI and Machine Learning
By Hitesh Raval, Principal Data Scientist & CDISC SME When submitting clinical trial data to regulatory agencies such as the FDA (U.S.) and PMDA (Japan), it is crucial to follow submission data standards, such as CDISC standards to ensure compliance. The manual mapping of data fields from a clinical trial database to the corresponding compliant […]
Journey from developer to innovator for generating clinical trial artifacts
By Amit Gupta, Technical Lead- Software Development My name is Amit Gupta, and currently I am working as a full stack developer and innovator at GenInvo for generating clinical trial artifacts with overall 10+ years of extensive IT experience. Interest in technology from the school days made me into the bachelor’s in computer science and […]
