Protocol Registration on ClinicalTrials.gov
About this Event
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Participants will have the opportunity to experience data entry within the ClinicalTrials.gov Protocol Registration System (PRS) system with guidance. This class is intended for those who are new to Protocol Registration data entry or need additional assistance in navigating the ClinicalTrials.gov Protocol Registration entry system.
Level: BEGINNER
Provider - Clinical Research Management & Support Office
Objectives
At the end of this ILT, participants will be able to:
· Distinguish the requirements per FDAAA, ClinicalTrials.gov, and ICJME and how to navigate the ClinicalTrials.gov Protocol Registration System.
· Identify the tools and documentation that are needed to facilitate the entry of the information into the ClinicalTrials.gov Protocol Registration System.
· Identify how to reduce the number of reviewer comments and minimize time with obtaining an NCT # from the ClinicalTrials.gov Protocol Registration System.
Event Details
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