Clinical Research Education Series (CRES) | “Regulatory Affairs Office: Updates on Services Provided for HMRI Sponsored Trials"
This presentation will provide a brief overview of updates and changes within the Regulatory Affairs Office. It will provide useful information regarding: Updates for services provided on HMRI sponsored trials, IND submissions for Investigator Initiated Trials, IDE submissions for Investigator Initiated Trials and other topics.
Target Audience
Employees at Houston Methodist Hospital Research Institute
Learning Objectives
Participant Learning Outcomes:
- Overview of the Regulatory Affairs Office and services provided
- IND submissions for Investigator Initiated Trials
- IDE submissions for Investigator Initiated Trials
- Investigator Responsibilities for IITs: FDA annual Reports & ClinicalTrials.gov
Virtual - ZOOM link with be provided to the registered participants.
Presenter Info:
- Raquel Bunge, RN, BSN, CCRC
- Rashawn Lee
- Yancey Lee
- Carlotta Borsoi
1.00 Attendance
Available Credit
- 1.00 Attendance
For Houston Methodist Employees:
If you are an employee of Houston Methodist and this is your first time accessing this site, you may proceed to register for your activity by following these steps:
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If you have previously created a profile, you may proceed to register for your activity by completing the above steps 1 & 2 and registering for your activity.
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- Update your mobile number.
If you have previously created a profile, you may proceed with registering for the activity by selecting “Log In.” Select “Visitor Log In,” and login with the information you previously used.
For additional information please visit the FAQ section.