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

 1

Human research participant protection programs (HRPPPs),

3

 1-1

Human research participant protection programs (HRPPPs),

37

 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