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UNIVERSITY OF PENNSYLVANIA COMBINED SUBJECT INFORMED CONSENT AND HIPAA AUTHORIZATION FORM Protocol Title:Cigar Packaging StudyPrincipal Investigator:Andrew A. Stressed, Ph.D. 3535 Market St., Suite
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01
Ensure the participant understands the purpose of the study or procedure.
02
Clearly explain the risks and benefits involved.
03
Allow the participant to ask any questions and address any concerns they may have.
04
Provide the participant with a written consent form to read and sign.
05
Make sure the participant is signing the form voluntarily and without any coercion.
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Keep a copy of the signed consent form for your records.

Who needs obtaining informed consent for?

01
Researchers conducting studies involving human subjects
02
Healthcare professionals performing medical procedures
03
Legal guardians for minors or individuals who are unable to give consent
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Obtaining informed consent is for ensuring that individuals understand and agree to participate in a research study or medical procedure.
Researchers, medical professionals, or institutions conducting the study or procedure are required to file obtaining informed consent.
Obtaining informed consent is typically filled out by providing information about the study or procedure, risks and benefits, and obtaining the individual's signature indicating they understand and agree.
The purpose of obtaining informed consent is to protect the rights and welfare of individuals participating in research studies or medical procedures.
Information reported on obtaining informed consent typically includes study or procedure details, risks and benefits, participant rights, and researcher contact information.
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