What is an Informed Consent Form?
This is a form that ensures that you have consented to participate in the clinical study. The Informed Consent process is a dialogue between you and the study doctor and/or nurse about the study procedures, benefits, and risks. This discussion takes place before you agree to join the study. You will be given a consent form to read. You should ask questions about any part of the consent form you do not understand. If you decide to take part in the study, you will be asked to sign the consent form. Even if you sign these forms, you can change your mind and stop participating in the study at any time. Regulatory authorities, such as the Food and Drug Administration (FDA) in the US, require that clinical trial volunteers sign an informed consent form that has been previously reviewed and approved by an Institutional Review Board (IRB) before entering a study. In Canada, an Ethics Committee reviews this form. These groups are independent review boards responsible for protecting the rights o
This is a form that ensures that you have consented to participate in the clinical study. The Informed Consent process is a dialogue between you and the study doctor and/or nurse about the study procedures, benefits, and risks. This discussion takes place before you agree to join the study. You will be given a consent form to read. You should ask questions about any part of the consent form you do not understand. If you decide to take part in the study, you will be asked to sign the consent form. Even if you sign these forms, you can change your mind and stop participating in the study at any time. Regulatory authorities, such as the Food and Drug Administration (FDA) in the US, require that clinical trial volunteers sign an informed consent form that has been previously reviewed by an Institutional Review Board (IRB) before entering a study. In Canada, an Ethics Committee reviews this form. These groups are independent review boards responsible for protecting the rights of those parti
This document provides you with a detailed description of the clinical study. Your signature on the informed consent form signifies that you have been provided with information about the study, that you understand the risks and benefits of the study, and that you are willing to participate in the study. Participation is entirely voluntary and you may stop participating in the study at any time.
This is a document that provides you with a detailed description of the clinical study. Your signature on the informed consent form documents that you have been provided with information about the study, that you understand the risks and benefits of the study, and that you are willing to participate in the study. Participation is entirely voluntary. You may stop participating in the clinical research study at any time.
