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Information and Consent Form For Adults Aged 18 and Older Additional Facility Sites Sanofi Pasteur Inc. STA00011INFORMATION AND CONSENT FORM For Adults Aged 18 and Older Additional Facility Sites
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Submit the completed form to the appropriate recipient

Who needs information and consent form?

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Individuals participating in research studies
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Patients receiving medical treatment
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Employees in certain workplaces
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An information and consent form is a document that outlines the details of a study or medical procedure, providing participants with necessary information and obtaining their consent to participate.
Researchers or organizations conducting studies involving human participants are required to file an information and consent form.
To fill out an information and consent form, provide clear information about the study, including its purpose, procedures, risks, benefits, and ensure that participants can ask questions before signing.
The purpose of the information and consent form is to inform participants about the nature of the study and to obtain their voluntary agreement to participate.
The form must include details such as the study's purpose, procedures involved, potential risks, benefits, confidentiality assurances, and contact information for questions.
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