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Document Number: SOP×01/V3 Title: Obtaining Informed Consent and Assent for Research Studies Author: Pam Dicks×Susan Macfarlane Effective Date: 27 Feb 2013 Periodic Review Date: 26 Feb 2016 Superseded
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How to fill out obtaining informed consent for

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How to fill out obtaining informed consent for:

01
Start by clearly identifying the purpose of the informed consent form. This could include specifying the research study, medical procedure, or any other relevant activity requiring consent.
02
Include a detailed explanation of the risks and benefits associated with the activity. This information should be presented in a clear and understandable manner, ensuring that the individuals giving consent are fully aware of what they are agreeing to.
03
Clearly outline any alternatives that individuals have, presenting them with other options if applicable. This allows them to make informed decisions about their participation or alternative courses of action.
04
Include a section for individuals to ask questions or seek clarification before signing the consent form. This ensures that all their concerns are addressed and that they have a complete understanding of what they are consenting to.
05
Make sure to include a section where individuals can provide their signature and the date of consent. This signature serves as proof that they have willingly and voluntarily agreed to participate or undergo the specific activity.

Who needs obtaining informed consent for:

01
Medical professionals and researchers conducting clinical trials or medical procedures on patients need to obtain informed consent. This ensures that patients understand the risks, benefits, and alternatives before undergoing any treatments or procedures.
02
Educational institutions or researchers conducting experiments, surveys, or studies involving human participants need to obtain informed consent. This ensures that participants are aware of the purpose, risks, and benefits of their involvement and have the opportunity to withdraw their consent at any time.
03
Any organization or entity that collects personal information from individuals, such as for marketing purposes or data analysis, may need to obtain informed consent. This ensures that individuals are aware of how their information will be used and shared, giving them the option to provide consent or withhold it.
It is important to note that the specific requirements for obtaining informed consent may vary depending on the jurisdiction and the nature of the activity. It is always recommended to consult local laws and regulations to ensure compliance.
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Obtaining informed consent is for ensuring that a person fully understands the risks and benefits of a decision before giving consent.
Healthcare professionals, researchers, or individuals who are conducting research or administering medical treatments are required to obtain informed consent.
Obtaining informed consent is typically filled out by providing detailed information about the procedure or research, risks involved, benefits, and allowing the individual to ask any questions.
The purpose of obtaining informed consent is to respect the autonomy and rights of individuals, ensure they have the information needed to make an informed decision, and protect them from potential harm.
The information reported on obtaining informed consent includes details about the procedure or research, risks and benefits involved, alternatives, and the individual's right to withdraw consent at any time.
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