ClinicalTrials.gov Advanced Reporting

This course will engage the participant in an interactive practical workflow for entering study results in ClinicalTrials.govPRS (Protocol Registration System). The participant will enter results for study interventions including: Parallel, Crossover and Factorial design. The user will master results entry for the four results entry modules including the addition of Statistical Analysis and scenarios for troubleshooting results template issues.***This class is restricted to experienced users and requires completion of the ClinicalTrials.gov Results Reporting Class as a prerequisite. ***