Presentations to the IRB

Date	Presentations Provided to IRB Members
Aug 2015	• Non-compliance [1]
July 2015	• Component Analysis [2]
June 2015	• Children's Findings Signature Requirements [3]
May 2015	• Children's Findings [4]
Apr 2015	• Recruitment [5]
Mar 2015	• Additional Documentation Needed for Approval [6]
Feb 2015	• Non-Significant Risk Devices [7]
Jan 2015	• Scientific & Scholarly Validity [8]
Dec 2014	• IRB Member Conflicting Interests [9]
Nov 2014	• CoI: Action Reports & Management Plans [10]
Oct 2014	• Waiver of Documentation of Consent (waiver of signature) [11]
Sept 2014	• Waivers and Alterations of Consent [12]
Aug 2014	• HIPAA [13]
July 2014	• Privacy vs. Confidentiality [14] ()
June 2014	• Expedited Review [15]
May 2014	• Unanticipated Adverse Device Effect (UADE) [16]
Apr 2014	• IRB Member Conflict of Interest (CoI) [17]
Mar 2014	• Non-Significant Risk Devices [18]
Feb 2014	• Conflict of Interest: Action reports & Management plans [19]
Jan 2014	• Scientific Review & Scholarly Validity [20]
Dec 2013	• Mobile Medical Apps [21]
Nov 2013	• Recruitment [22]
Oct 2013	• Waiver of Informed Consent [23]
Sept 2013	• Waiver of Documentation (or signature) of informed consent [24]
Aug 2013	• Preparing For AAHRPP: Criteria for Approval [25] (Part 2)
July 2013	• Preparing For AAHRPP: Criteria for Approval [26] (Part 1)
June 2013	• Preparing For AAHRPP: Unanticipated Problems [27]
May 2013	• Preparing For AAHRPP: Non-Compliance [28]
Apr 2013	• Preparing For AAHRPP: Expedited Review [29]
Mar 2013	• Preparing For AAHRPP: the Role of the IRB Member [30]
Feb 2013	• Preparing For AAHRPP: Introduction [31]
Jan 2013	• Waiver of Documentation [32]
Dec 2012	• Equitable Selection [33]
Nov 2012	• Criteria for IRB Approval of Research [34] (Part 2) ()
Oct 2012	• Criteria for IRB Approval of Research [35] (Part 1) ()
Sept 2012	• Recruitment [36] ()
Aug 2012	• Expedited Review Revisited [37] ()
July 2012	• Clinical Radiation Safety - Research with Children [38] ()
May 2012	• Human Subjects Protocols: Privacy Considerations [39] ()
April 2012	• Children's Findings – Assent and Permission [40] () • Children's Findings – Assent and Permission [41] ()
March 2012	• Expanded Access [42] () • Expanded Access [43] ()
Feb 2012	• Pregnant Women [44] () • Pregnant Women [45] ()
Jan 2012	• Phone Scripts, Questionnaires and Waivers of Documentation of Consent [46] () • Phone Scripts, Questionnaires and Waivers of Documentation of Consent [47] ()
Dec 2011	• Regulations for SCRO Clinical Trials and ClinicalTrials.gov [48] () • Additional Element of Consent: ClinicalTrials.gov [49] () • Additional Element of Consent: ClinicalTrials.gov [50] ()
Nov 2011	• Informed Consent Requirements and Elements - Revisited [51] () • Informed Consent Requirements and Elements - Revisited [52] ()
Oct 2011	• Provenance in Stem Cell Research [53] ()
Aug 2011	• Issues with Tissues [54] () • Issues with Tissues [55] ()
Jul 2011	• Events & Information that Require Prompt Reporting to the IRB [56] ()
May 2011	• Unanticipated Problems (UPs) & Adverse Events (AEs) "more info" [57] ()
Apr 2011	• Informed Consent Scenarios [58] (Medical, ) • Informed Consent Scenarios [59] (Non-Medical, )
Mar 2011	• Genetic Research: Basic Vocabulary and Terminology [60] ()
Feb 2011	• Data Safety Monitoring and the IRB [61] ()
Jan 2011	• Scientific and Scholarly Review [62] ()
Dec 2010	• Criteria for IRB Approval of Research [63] ()
Nov 2010	• Prisoner Research and the IRB [64] ()
Oct 2010	• Vulnerable Populations and Human Subjects Review [65] ()
Sept 2010	• Research Involving Children and Radiation Exposure [66] ()
Aug 2010	• (A) Determination of Human Subject Research; [67] (B) Exempt Categories [67] () • [SCRO] Updates to Stem Cell Research Oversight [68] ()
Jul 2010	• Certificates of Confidentiality (CoC) [69] ()
Jun 2010	• IRB Quiz [70] ()
May 2010	• Children in Research [71] (Medical, ) • Children in Research [72] (Non-Medical, )
Apr 2010	• Expedited Review [73] ()
Mar 2010	• Guidance on Unanticipated Problems (UPs) and Adverse Events (AEs) [74] (Medical, ) • Guidance on Unanticipated Problems (UPs) and Adverse Events (AEs) [75] (Non-Medical, ) • CIRM Disease Team MPP Grants [76] (Presentation to IRB 3/SCRO, )
Feb 2010	• Ethnographical Research [77] (Non-Medical, )
Jan 2010	• General Requirements for Informed Consent [78] (Medical, ) • General Requirements for Informed Consent [79] (Non-Medical, ) • SCRO Consent Requirements [80] () • Stem Cell Terminology [81] ()
Dec 2009	• Short Form Consent Process [82] () • Sponsor-Investigator Research [SIR] and Investigational New Drugs [INDs] [83] ()
Nov 2009	• Criteria for IRB Approval of Research [84] (Medical, ) • Criteria for IRB Approval of Research [85] (Non-Medical, ) • A Guide for the Combined IRB/SCRO [86] ()
Oct 2009	• IRB Member Orientation [87] () • Resources Supporting the HRPP [88] ()
Sept 2009	• Funding Research [89] ()
Aug 2009	• HIPAA [90] ()
July 2009	• Understanding Waivers & Alterations of Consent [91] ()
Jun 2009	• Laboratory Employees and Students as Research Subjects [92] ()
May 2009	• Belmont Report - History, Principles and Application [93] ()
Apr 2009	• IRB Determinations about Parental Permission [94] ()
Mar 2009	• Additional Protections for Pregnant Women, Fetuses and Neonates [95] () • Survey Research in Public Schools [96] (PPRA Regulation, )
Jan 2009	• AAHRPP Site Visit - December 2008 [97] ()