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This document serves as an informed consent form for participants in the Multi-Institutional Neo-adjuvant Therapy MammaPrint Project I (MINT I Study), providing essential information regarding the

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What is informed consent to participate?

Informed consent to participate refers to the process by which individuals are fully informed about the details and potential risks of a study or research before agreeing to participate. It ensures that participants have a clear understanding of what is expected of them and gives them the opportunity to ask questions and make an informed decision about whether they want to participate or not.

Who is required to file informed consent to participate?

Researchers, organizations, or individuals conducting a study or research are required to obtain and file informed consent to participate from the individuals they wish to include as participants. This ensures that participants are fully aware of the study's purpose, procedures, and any potential risks or benefits before giving their consent.

How to fill out informed consent to participate?

Informed consent forms can vary depending on the study or research being conducted, but they typically include sections such as a description of the study, its purpose, procedures, risks, benefits, confidentiality, voluntary participation, and contact information for any questions or concerns. Participants are required to read and understand the information provided and then sign the form to indicate their voluntary consent.

What is the purpose of informed consent to participate?

The purpose of informed consent to participate is to protect the rights and well-being of individuals participating in a study or research. It ensures that participants are fully informed about the study's objectives, procedures, potential risks, and benefits, and gives them the opportunity to make an autonomous decision about their participation. Informed consent also promotes transparency, honesty, and ethical conduct in research.

What information must be reported on informed consent to participate?

Informed consent forms typically require researchers to provide information such as the study's purpose, procedures, potential risks and benefits, expected duration, confidentiality measures, voluntary participation, contact information for questions or concerns, and any compensation or incentives offered. Additionally, the form may include language explaining the participant's right to withdraw from the study at any time without repercussions.