References
Listed below is all the known content in the system that links to this item.
1.29 ClinicalTrials.gov Reporting
HRPP Policies and Procedures
Section 1: General Human Research Prote...
1.0. Purpose The purpose of this policy is to describe the requirements for registration and com...
2.2 Full IRB Review
HRPP Policies and Procedures
Section 2: Process of Review
1.0 Purpose The purpose of this policy is to describe the Organization’s requirements for: 1) sub...
2.3 Expedited Review
HRPP Policies and Procedures
Section 2: Process of Review
1.0 Purpose The purpose of this policy is to describe the Organization’s requirements for using e...
2.4 IRB Review of Changes in Previously Approved Research
HRPP Policies and Procedures
Section 2: Process of Review
1.0 Purpose The purpose of this policy is to describe the Organization’s requirements for IRB rev...
2.7 Continuing Review of Research
HRPP Policies and Procedures
Section 2: Process of Review
1.0 Purpose The purpose of this policy is to describe the Organization’s requirements for continu...
5.1 Obtaining Informed Consent From Research Subjects
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 pro...