Office of Research Integrity

Archives to Prior Version of Revised Policies and Superceeded Policies

Superceeded Policies

IRB Policies and Procedures - Entire Guide Superceeded 11/01/2008

Revised Policy and Procedures - Prior Policy Versions

Effective Date
Date Archived
HRPP 1.1 - Description, Principles and Authority for MUSC HRPP
12/01/2009
10/01/2010
01/27/2012
HRPP 1.2 - MUSC Organization
01/27/2012
HRPP 1.3 - Definitions of Terms
01/27/2012
01/27/201205/08/2013
HRPP 1.4 - Scientific/Scholarly Review of Protocols Policy and Procedures
01/27/2012
HRPP 1.5 - State Laws Affecting Human Subjects Research
01/27/2012
HRPP 1.6 - Communicating Conflict of Interest (COI)
01/27/2012
HRPP 2.1 - Responsibilities Ethical Principal Authority and Independence of the IRB
01/27/2012
HRPP 2.2 - Functions of the IRB
01/27/2012
HRPP 2.3 - Membership of the IRB
01/27/2012
05/15/2012
08/01/2012
HRPP 2.4 - Approval of Research activities by the IRB
01/27/2012
HRPP 2.5 - Convened Meetings of the IRB
01/27/2012
05/15/2012
HRPP 2.6 - Retention of Review Activities Records of the IRB
01/27/2012
HRPP 2.7 - Management of the IRBs
01/27/2012
HRPP 3.1 - Human and Not Human Research Policy and Procedures
12/01/2009
01/27/2012
HRPP 3.2 - Exempt Research Review Policy and Procedures
01/27/2012
01/27/201209/16/2013
HRPP 3.3 - Expedited Research review Policy and Procedures
12/01/2009
01/27/2012
HRPP 3.4 - Full Board Initial Review Policy and Procedures
01/27/2012
HRPP 3.5 - Full Board Continuing Review Policy and Procedures
01/27/2012
HRPP 3.6 - Full Board Amendment Policy and Procedures
01/27/2012
HRPP 3.8 - Quality Improvement Projects Policy and Procedures
01/27/2012
HRPP 4.1 - Review of Research involving Drugs or Biological Drug Products
01/27/2012
HRPP 4.2 - Single Emergency Use of an Investigational Drug
01/27/2012
HRPP 4.3 - Review of Research Involving Medical Devices
01/27/2012
08/01/2012
HRPP 4.4 - Medical Devices Risk Determination Policy and Procedures
12/01/2009
01/27/2012
HRPP 4.5 - Emergency Use of an Investigational Device Policy and Procedures
01/27/2012
01/27/201205/08/2013
HRPP 4.6 - Humanitarian Use Device
01/27/2012
01/27/ 201205/08/2013
HRPP 4.7 - Unanticipated Problems and Adverse Events Policy and Procedures
10/01/2010
01/27/2012
08/01/2012
HRPP 4.8 - Management of Non-Compliance Policy and Procedures
01/27/2012
01/27/201208/08/2013
HRPP 4.9 - Suspension or Termination of IRB-Approved Research
01/27/2012
01/27/201208/08/2013
HRPP 4.10 - Data and Safety Monitoring Plans
01/27/2012
HRPP 4.11 - Human Gene Transfer Studies Policy and Procedures
12/01/2009
01/27/2012
HRPP 4.12 - Clinical Trials Registration
01/27/2012
HRPP 4.13 - Privacy and Confidentiality
12/01/2009
01/27/2012
HRPP 4.14 - Protocol Deviation Policy and Procedures
01/27/2012
HRPP 5.1 - Principal Investigator Responsibilities - Supervision of Staff and Protection of Subjects
11/15/2009
01/27/2012
HRPP 5.2 - Principal Investigator Responsibilities - Recordkeeping and Record Retention
01/27/2012
HRPP 5.3 - Education and Training Requirements for Individuals Involved in Human Research
01/27/2012
08/01/2012
08/01/201201/31/2013
HRPP 6.1 - Informed consent to Participate in Research Policy and Procedures
04/27/2010
09/22/2010
10/13/2010
01/27/2012
HRPP 6.2 - Hyperlinks to IRB Informed Consent Information and Guidance
01/27/2012
HRPP 7.1 - Equitable Selection of Subjects
01/27/2012
HRPP 7.2 - Advertisements for Research Participations Policy and Procedures
01/27/2012
HRPP 7.3 - Payments for participation Policy and Procedures
01/24/2009
01/27/201204/01/2013
HRPP 7.5 - Research Involving Non-English Speaking Subjects Policy and Procedures
01/27/2012
HRPP 7.6 - Research Subject Advocacy Policy and Procedures
01/27/2012
09/17/2012
HRPP 7.7 - Subject Complaints, Issues, Concerns and Suggestions Policy and Procedures
01/27/2012
HRPP 8.1 - Vulnerable Populations - General Guidelines
03/03/2010
01/27/2012
HRPP 8.2 - Research Involving Persons with impaired Decision Making Capacity
01/27/2012
HRPP 8.3 - Research involving Prisoners
01/27/2012
HRPP 8.4 - Research Involving Pregnant Women, Fetuses, and Neonates
01/27/2012
HRPP 8.5 - Research Involving Children
01/27/2012
05/15/2012
HRPP 9.1 - Multi-Site Research Studies Policy and Procedures
10/01/2010
01/27/2012
HRPP 9.2 - Management of Reporting events in Multi-Site Research Studies
01/27/2012
HRPP 9.3 - Transnational Studies Policy and Procedures
05/15/2012
08/01/2012
HRPP 10.1 - Human Research Audit
10/01/2010
10/15/2011
HRPP 10.2 - Record Retention Policy
01/27/2012
HRPP 10.3 - Quality Improvement Initiatives
01/27/2012