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Get the free ConnectED Informed Consent - Sites at Penn State

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CONSENT TO PARTICIPATE IN RESEARCH IRB Protocol ID: Principal Investigator: 45866 Barbara E. Each Lee R. Glatfelter Library, Penn State York, 1031 Edge comb Ave., York, PA 17403 7177714023; bee11
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Begin by carefully reading the document to understand the purpose and scope of the connected informed consent.
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Review the specific permissions and authorizations required, and indicate your agreement by ticking the appropriate boxes or signing where necessary.
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Who needs connected informed consent:

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Patients or research participants who are involved in studies or clinical trials that utilize connected medical devices or technologies.
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Any individual who is engaging in a healthcare service that involves the use of connected devices or technologies.
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Researchers, healthcare professionals, or organizations conducting studies or implementing connected healthcare solutions that require informed consent from participants.
Note: It is important to consult with legal and healthcare professionals to ensure compliance with all relevant laws, regulations, and ethical considerations when filling out connected informed consent forms.
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Connected informed consent is a process in which a person gives permission for their data to be shared and used in a connected manner.
Anyone who collects or shares data in a connected way is required to file connected informed consent.
Connected informed consent can be filled out by providing relevant information about the data being shared, the purpose of sharing, and obtaining explicit consent from the individual.
The purpose of connected informed consent is to ensure that individuals are aware of how their data is being shared and used in a connected environment.
Information such as the type of data being shared, the entities involved in sharing, the purposes of sharing, and consent status must be reported on connected informed consent.
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