LIST OF TABLES, FIGURES, AND BOXES

Tables

 1

 

Comparison of Draft NCQA and PRIM&R Accreditation Standards,

 

8

 3-1

 

Elements in Three Sets of Standards and Guidelines,

 

78

 C-1

 

Draft Accreditation Outcomes and Remedial Action,

 

138

 C-2

 

Institutional Reponsibilities,

 

145

 C-3

 

Individual IRB Structure and Operations,

 

156

 C-4

 

Considerations of Risks and Benefits,

 

171

 C-5

 

Recruitment and Subject Selection,

 

177

 C-6

 

Privacy and Confidentiality,

 

180

 C-7

 

Informed Consent,

 

183

Figures

 1

 

Human research participant protection programs (HRPPPs),

 

3

 1-1

 

Human research participant protection programs (HRPPPs),

 

37

Boxes

 1

 

Summary of Committee's Recommendations According to the Three Implementation Phases of an Accreditation Process,

 

22

 1-1

 

Relevant International Codes,

 

27

 3-1

 

The International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use,

 

85

 A-1

 

Organizations and Individuals Appearing Before the Committee,

 

106



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