Clinical Trials Resource Center
Search

Clinical Trial Services
Protocol Development
Consent Development
Recruitment Strategy
Budgeting
Data & Safety Monitoring
Safety Reporting
Quality Management
Study Management
 
Clinical Trial Services
li
IND / IDE Submissions
li
ClinicalTrials.Gov Registration
FDA Inspection
Validation and Compliance with 21 CFR Part 11
Clinical Trial Services
li
Mission, Vision and Goals
li
Staff
li
Home
Visit the Center for Clinical & Translational Sciences


Clinical Trial Services
Investigators
Study Staff
Partners
Participants
 
Clinical Trial Services
Clinical Trial Budgeting
Clinical Research Coordinator Course
Good Clinical Practice Training
UT Health Investigator Courses
Clinical Research Forum
Human Subjects Training
li
iRIS Training

Clinical Trial Services
li
GCP Guidance
li
Federal Regulations
li
Human Subjects Protection Program
li
ICH GCP Guidelines
li
Newsletter
li
*Quick Reference*
|| IQ BOX ||


 

NOTICE OF UTHSC SITE INSPECTION

Please fill out this form immediately upon notification of a site inspection by a regulatory authority. 

PI's Name

Study Title and IRB Number:

UTHSC Department and Main Contact
 

Date(s) of Inspection: (mm/dd/yy)

Who is Conducting the Inspection: (e.g., CDER/FDA)

Work Phone : 
Email Address: 

Is this For Cause? Any other relevant Information:

 

Upon submission, this will distribute a notification to designees within the departments of CPHS, CTRC, Institutional Compliance, and Auditing and Advisory Services.

 
Your Portal to Best Practices in Clinical Trial Management
EMAIL: CLINICALTRIALS@UTH.TMC.EDU PHONE: 713-500-3622 FAX 713-500-0334
University of Texas Houston Health Science Center Logo