References materials

6.1 HISTORY and LANGUAGE

	6.1.01.	Daniel
	6.1.02A	Acronyms 2009
	6.1.02B	IRC Glossary 2009
	6.1.03	NBAC Independent IRB History

6.2 REGULATIONS

	6.2.01	45 CFR 46-The Common Rule
	6.2.02	21 CFR 56 IRB
	6.2.03	21 CFR 50 FDA Informed Consent

6.3 CODES OF ETHICS
We try to keep these up to date. If you are quoting or using them officially, please go to the original site.

	6.3.01	Nuremberg Code
	6.3.02	Helsinki 2000
	6.3.03A	The Belmont Report
	6.3.03B	The Belmont Report-Appendices
	6.3.04A	ACRP
	6.3.04B	CIRB
	6.3.04C	AMA

6.4 GUIDANCE DOCUMENTS
The FDA and OHRP websites are better sources of their guidance documents.

6.5 Reading materials
Being updated

6.6 Educational resources
Places to get required or recommended training in Good Research Practices.

	6.6	Education and Training Resources
	6.6.1	Late Phase Demo (from outside IRC)
	6.6.2	Late Phase Demo (from inside IRC)
	6.6.3	Late Phase SELF-DEMO (from outside IRC)
	6.6.4	Late Phase SELF-DEMO (from inside IRC)
	6.6.5	Late Phase PowerPoint
	6.7	SmartForms (link from outside IRC)
	6.8	SmartForms (link from inside IRC)

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6.8 ---

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