Clinical Research Education Series (CRES) | “An Introduction to ClinicalTrials.gov"

March 25, 2026

This session will introduce ClinicalTrials.gov and its role in clinical research transparency and regulatory compliance. Participants will learn which studies require registration, key reporting timelines, and common compliance considerations. The presentation will also review the responsibilities of research teams in maintaining accurate study records and highlight resources available to support ClinicalTrials.gov compliance.

 

Target Audience

Employees at Houston Methodist Hospital Research Institute 

Learning Objectives

Participant Learning Outcomes

  • Recognize which studies require registration in ClinicalTrials.gov.
  • Understand key registration and results reporting timelines.
  • Identify common compliance risks related to ClinicalTrials.gov reporting.
  • Understand the role of research teams in maintaining accurate and timely study records.
Course summary
Available credit: 
  • 1.00 Attendance
Course opens: 
03/16/2026
Course expires: 
03/25/2026
Event starts: 
03/25/2026 - 12:00pm CDT
Event ends: 
03/25/2026 - 1:00pm CDT
Add to calendar: 
Virtual Meeting
Houston, TX
United States

Virtual - ZOOM link with be provided to the registered participants.

Presenter(s) Info:

 Rosbel Brito, MPH, CCRP, ECFMG-certified

&

Carlotta Borsoi, MS, MCTM

1.00 Attendance

Available Credit

  • 1.00 Attendance
Please login or register to take this course.

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