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Ethical Research Practice
Institutional Review Board
IRB Review Criteria

Informed Consent
--Capacity to Consent
--Freedom from Coercion
--Risks & Benefits
--Informed Consent Document
--Informed Consent Delivery
--Waiver of Informed Consent
--Quiz

Genetic Testing
Types of Review
Continuation & Final Reports
Serious Adverse Events
Frequently Asked Questions
Conclusion

Informed Consent Delivery

The process of informed consent also involves the research investigator or assistants explaining any aspect of the study to the patient’s fullest understanding. This process takes time and can occur throughout the investigation, but initial understanding allows the patient to make an informed decision as to whether they wish to participate in the study.

Subjects should be given adequate time to read and understand the informed consent and given a copy of the informed consent. At any point during the research, they should be able to contact the primary researchers and research assistants and receive answers to questions they may have.

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