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1.8 Investigational Activities Requiring IRB Review and Approval
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1.22 Assessment of the Effectiveness and Efficiency of the HRPP
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8.4 Review of Noncompliance Involving the PI or Study Personnel
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6.5 Expanded Access to Investigational Drugs and Devices for Treatment Use
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5.2 Waiver or Alteration of Informed Consent and HIPAA Authorization
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Robert A Lewis
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6.5 Expanded Access to Investigational Drugs and Devices for Treatment Use
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Robert A Lewis
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5.2 Waiver or Alteration of Informed Consent and HIPAA Authorization
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Emergency Preparedness /Continuity of Operations Plan (EP/COOP)
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Robert A Lewis
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1.6 IRB Composition, Leadership, Qualifications, and Responsibilities
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Robert A Lewis
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Emergency Preparedness /Continuity of Operations Plan (EP/COOP)
HRPP Policies and Procedures
1.0 Emergency Preparedness /Continuity of Operations Plan (EP/COOP) 1.1. Purpose The UNMC Offi...
1.34 Emergency Preparedness for the Office of Regulatory Affairs and IRBs
HRPP Policies and Procedures
Section 1: General Human Research Prote...
1.0 Purpose The purpose of this policy is to describe the Emergency Preparedness and Continuity ...
5.7 Obtaining Informed Consent from Non-English Speaking Persons, or Persons with Additional Needs or Vulnerabilities
HRPP Policies and Procedures
Section 5: Informed Consent
1.0 Purpose The purpose of this policy is to describe the Organization’s requirements for the pr...
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