A selection of presentations to the Stanford research community, and IRB members and staff. Comments or suggestions? Contact IRB Education or call (650) 724-7141. Click on "Topic" or "Title" to sort this list. Topic Title (pdfs) Certificates of Confidentiality Certificates of Confidentiality (CoC) (Jul 2010) Children Children in Research (Medical) (May 2010) Children in Research (Non-Medical) (May 2010) Children Research involving Children and Radiation Exposure (Sep 2010) Consent Informed Consent - Requirements and Documenting (Mar 2010) Consent Short Form Consent Process (Dec 2009) Consent General Requirements for Informed Consent (Medical) (Jan 2010) General Requirements for Informed Consent (Non-Medical) (Jan 2010) Consent Understanding Waivers & Alterations of Consent (Jul 2009) Data Safety Monitoring Data Safety Monitoring and the IRB (Feb 2011) Ethics Belmont Report - History, Principles and Application (May 2009) General Funding Research (Sep 2009) General Resources Supporting the HRPP (Oct 2009) HIPAA HIPAA (Aug 2009) IRB Process IRB Overview (Jul 2009) IRB Process IRB Annual Update (May 2009) IRB Process Criteria for IRB Approval of Research (Medical) (Nov 2009) Criteria for IRB Approval of Research (Non-Medical) (Nov 2009) IRB Process Determination of Human Subject Research (Aug 2008) IRB Process Exempt Review Categories (Aug 2008) IRB Process IRB Quiz (Jun 2010) Reporting Events & Information that Require Prompt Reporting to the IRB (July 2011) Reporting Unanticipated Problems (UPs) & Adverse Events (AEs) (Medical) (Mar 2010) Unanticipated Problems (UPs) & Adverse Events (AEs) (Non-Medical) (Mar 2010) Reporting Unanticipated Problems (UPs) & Adverse Events (AEs) "more info" (May 2011) Special Populations Laboratory Employees and Students as Research Subjects (Jun 2009) Special Populations Vulnerable Populations and Human Subjects Review (Oct 2010) Sponsor-Investigator Research Sponsor-Investigator Research [SIR] & Investigational New Drugs (Mar 2011) Sponsor-Investigator Research Sponsor-Investigator Research [SIR] & Investigational New Drugs (Dec 2009) Tissue Issues with Tissues (May 2011)
A selection of presentations to the Stanford research community, and IRB members and staff.
Comments or suggestions? Contact IRB Education or call (650) 724-7141.
Click on "Topic" or "Title" to sort this list.
Certificates of Confidentiality
Certificates of Confidentiality (CoC) (Jul 2010)
Children
Children in Research (Medical) (May 2010) Children in Research (Non-Medical) (May 2010)
Research involving Children and Radiation Exposure (Sep 2010)
Consent
Informed Consent - Requirements and Documenting (Mar 2010)
Short Form Consent Process (Dec 2009)
General Requirements for Informed Consent (Medical) (Jan 2010) General Requirements for Informed Consent (Non-Medical) (Jan 2010)
Understanding Waivers & Alterations of Consent (Jul 2009)
Data Safety Monitoring
Data Safety Monitoring and the IRB (Feb 2011)
Ethics
Belmont Report - History, Principles and Application (May 2009)
General
Funding Research (Sep 2009)
Resources Supporting the HRPP (Oct 2009)
HIPAA
HIPAA (Aug 2009)
IRB Process
IRB Overview (Jul 2009)
IRB Annual Update (May 2009)
Criteria for IRB Approval of Research (Medical) (Nov 2009) Criteria for IRB Approval of Research (Non-Medical) (Nov 2009)
Determination of Human Subject Research (Aug 2008)
Exempt Review Categories (Aug 2008)
IRB Quiz (Jun 2010)
Reporting
Events & Information that Require Prompt Reporting to the IRB (July 2011)
Unanticipated Problems (UPs) & Adverse Events (AEs) (Medical) (Mar 2010) Unanticipated Problems (UPs) & Adverse Events (AEs) (Non-Medical) (Mar 2010)
Unanticipated Problems (UPs) & Adverse Events (AEs) "more info" (May 2011)
Special Populations
Laboratory Employees and Students as Research Subjects (Jun 2009)
Vulnerable Populations and Human Subjects Review (Oct 2010)
Sponsor-Investigator Research
Sponsor-Investigator Research [SIR] & Investigational New Drugs (Mar 2011)
Sponsor-Investigator Research [SIR] & Investigational New Drugs (Dec 2009)
Tissue
Issues with Tissues (May 2011)
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