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INFORMED CONSENT From A Phase II Double blind Trial to Evaluate the Safety, Immunogenicity and Effect on Infant Immune Responses of a Single Dose of Trap in Pregnant Women in Mali Investigators:Center
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Read the informed consent form thoroughly to understand its purpose and the details needed.
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Complete the basic information section, including your name, address, and contact information.
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Provide your signature and date to acknowledge that you have understood the information and consent to participate.
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Answer any additional questions or sections that are relevant to the study or procedure.
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Review the completed form for accuracy and make any necessary corrections.
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Submit the filled-out informed consent form to the appropriate person or organization.

Who needs informed consent form a?

01
Individuals who are participating in research studies or medical procedures that require informed consent.
02
Patients who are receiving medical treatment, especially if it involves experimental or investigational interventions.
03
Minors or individuals who are unable to provide consent themselves, where a legal guardian or representative needs to fill out the form on their behalf.
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Informed consent form A is a document that ensures participants understand the nature, risks, and benefits of a study or medical procedure before agreeing to participate.
Researchers or institutions conducting studies involving human subjects are required to file informed consent form A.
To fill out informed consent form A, provide clear descriptions of the study, risks, benefits, voluntary participation, and obtain signatures from participants.
The purpose of informed consent form A is to protect the rights and welfare of participants by ensuring they are fully informed about their involvement in a study.
The information reported on informed consent form A includes the study's purpose, procedures, duration, risks, benefits, confidentiality, and the right to withdraw.
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