Speaker(s): 

Charles Brightbill, MS, CIP, CIM, Director, IRB Operations & HRPP, Geisinger – has nothing to disclose.

Moderator(s): 

Brenda Cook, MHSA, Research Compliance Analyst, Geisinger - has nothing to disclose. 

Learning Objectives: 

At the conclusion of this session, the participant should be able to: 

• Discuss the general requirements for informed consent.

• Identify and understand the elements of consent.

• Identify and understand consent processes, including, written consent, waiver of documentation of consent, and waiver, or alteration of consent,

• Discuss the requirements for parental permission, assent, and surrogate consent.

Disclosure of Relevant Financial Relationships with/without Commercial Interests:

The Planning Committee consisting of Lori Biacchi, David Carey, PhD, Candice Laubach, Sonia Lobo, PhD, Christin Spatz, MD, FASN, Rebecca Stoudt, DNP, PhD, CRNA and Brenda Cook, MHSA have no identified disclosures. 

CE Committee Member/Content Reviewers have nothing to disclose. 

Any/All relevant financial relationships have been mitigated. 

Content Disclosure: 

This presentation/content is HIPPA compliant. 

Commerical Support for this Session

None.