Blank informed consent form
[DOC File]INFORMED CONSENT DOCUMENT TEMPLATE: NON-MEDICAL
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CONSENT DOCUMENT FORMAT: To facilitate the IRB review process, the sample format below is recommended for consent forms. Prepare the entire document in 12 point type, with no blank pages or large blank spaces/paragraphs. Do not change the margins on the document. They are set to allow room for the IRB approval stamp.
[DOC File]INFORMED CONSENT FORM - Boston University
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Informed Consent Form. Information and Purpose: The interview for which you are being asked to participate in, is a part of a research study that is focused on examining the development of female collegiate tennis players. The researcher is also interested in the factors that keep players motivated to continue with tennis. The purpose of this ...
[DOCX File]Example Standard Operating Procedure for Informed Consent ...
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The informed permission/consent form will be reviewed with the potential participant’s parent(s)/LAR/guardian and each section will be addressed adequately and the main points will be highlighted. During the discussion, the potential participant’s parent(s)/LAR/guardian will be encouraged to ask questions or express any concerns he/she may ...
NIH INFORMED CONSENT TEMPLATE FOR EXPANDED …
This consent form describes the Expanded Access treatment and is designed to help you decide if you would like to receive this treatment. It provides important information about what you will be asked to do during the treatment, about the risks and benefits of the treatment, and about your rights.
[DOC File]SAMPLE CONSENT FORM
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Personal Copy of Consent Form: You may print (You will be provided with) a blank, unsigned copy of this consent form at the beginning of the study. Verification of Adult Age: By clicking “I Agree” below (By signing below), you attest that you are 18 years old or older. Verification of Informed Consent:
Informed Consent Form Template for clinical trials
The informed consent form consists of two parts: the information sheet and the consent certificate. 3. Do not be concerned by the length of this template. It is long only because it contains guidance and explanations which are for you and which you will not include in the informed consent forms that you develop and provide to participants in ...
[DOC File]Informed Consent - template - Churchill Hospital
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Recording Informed Consent. When the person taking consent is satisfied that the subject has been fully informed and understands what study participation entails, the consent form should be signed and dated by the subject and the authorised person who has conducted the discussion. All names should be printed clearly beneath the signatures.
Informed Consent Form Template for Clinical Studies
The informed consent form consists of two parts: the information sheet and the consent certificate. 3. Do not be concerned by the length of this template. It is long only because it contains guidance and explanations which are for you and which you will not include in the informed consent forms that you develop and provide to participants in ...
[DOCX File]Appendix K – Animal Owner/Client Informed Consent Form
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The purpose of this form is to secure an animal owner’s informed consent to enroll their animal(s) in non-terminal research/teaching protocols with the understanding that that the animal(s) remain the property of the owner/client and will be returned to the owner/client …
[DOCX File]Informed Consent Document Template and Guidelines
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For the purposes of this document, guidelines within the template will be provided in italics. If this document is used to develop your informed consent form, please remember to delete the italicized instructions and insert your specific information.
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