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PATIENT CONSENT FORM This completed form must be included with submission to the Journal of Pharmacy Practice and Research. Verbal consent is not sufficient.Title of Article: ___ Corresponding authors
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Read the informed consent form carefully to understand the purpose of the study and the risks involved.
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Sign and date the form to indicate your agreement to participate in the study.
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Who needs ide informed consent?

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Anyone who is participating in a clinical study that is regulated by the FDA and involves the use of investigational devices needs to fill out an IDE informed consent form.
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IDE informed consent refers to the document signed by a patient or subject participating in a clinical trial after being informed of the study's purpose, procedures, risks, and benefits.
Investigators conducting clinical trials are required to file IDE informed consent.
IDE informed consent is typically filled out by the investigator or a designated team member and must contain all necessary information required by regulatory authorities.
The purpose of IDE informed consent is to ensure that patients or subjects understand the risks and benefits of participating in a clinical trial and give their voluntary consent.
IDE informed consent must include details about the study's purpose, procedures, risks, benefits, confidentiality, and the participant's rights.
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kins collingwood jpprshpa au pharmacists applicable identifiable corresponding org submission relating authors releases

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