M.D. Anderson Events

Human Subjects Protection Training, day 1

Must register in the Education Center to attend this class.

This is day one of a three-half day presentation. We will focus on the history and ethics of clinical research, federal regulations, good clinical practice guidelines and institutional policies for research involving human subjects. Specific references addressed in the course include the Belmont Report, Declaration of Helsinki, Nuremberg Code, Food Drug & Cosmetic Act, Titles 21 and 45 of the Code of Federal Regulations, the International Conference on Harmonization Good Clinical Practice Guidelines, HIPAA regulations and institutional policies.  

The NIH mandates this education for all key personnel on grants. All new faculty and fellows are required to complete this course, regardless of previous clinical research experience. Once the course has been successfully completed, new faculty/fellows will be awarded research privileges, allowed to submit clinical trials for IRB review and approval and allowed to enroll patients on clinical trials. Be sure to register for all three days of this course.

Those individuals completing the Clinical Research Training for Staff will be awarded credit for this offering and do not need to register for this class separately. 

**Class locations may be verified by e-mailing researcheducation@mdanderson.org**

Date: 11/3/09, 8am to 11am
Time: 11/3/09, 8am to 11am
Location: Cancer Prevention Building, Floor 8, Rooms 5-8
Format: Training/Employee Development
Contact: Office of Research Education & Regulatory Management - (713) 563-5467 - researcheducation@mdanderson.org
Attachments:
  Tab 1.pdf (PDF, 1.7 MB)

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