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Obtaining Legally Effective Informed Consent

Before research activities may begin check that the following items are complete:

1 ) Confirm that the consent being presented to the subject is the currently approved IRB version
2 ) The form must be signed and dated by the subject where indicated
3)  The form must be signed and dated by the investigator or designee where indicated
4)  Make sure that all blank lines/checkboxes are appropriately completed by the subject


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