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CONJOINT HEALTH RESEARCH ETHICS BOARD CONSENT FORM TEMPLATETemplate Instructions:Delete this boxed information, all instructional text in red, and any sections of the consent template that are not
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How to fill out minimal risk information sheet

01
To fill out a minimal risk information sheet, follow these steps:
02
Start by providing your personal information such as your full name, date of birth, address, and contact details.
03
Specify the purpose of the information sheet and the timeframe it covers.
04
List any medical conditions or allergies you may have.
05
Include information about any medications or treatments you are currently undergoing.
06
Provide details about your emergency contact person, including their name, relationship to you, and contact information.
07
Include any additional relevant information or instructions.
08
Double-check all the details you have provided to ensure accuracy.
09
Sign and date the information sheet to confirm its authenticity.

Who needs minimal risk information sheet?

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A minimal risk information sheet is typically required by individuals participating in research studies or clinical trials.
02
It is used to collect necessary information about participants' personal and medical history, ensuring their safety during the study.
03
Other individuals who may need a minimal risk information sheet include patients visiting healthcare facilities for treatment or procedures, where their medical history and potential risks need to be documented.

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A minimal risk information sheet is a document that provides information on low-risk activities or studies that pose minimal harm or danger to participants.
Researchers or institutions conducting low-risk studies or activities are required to file a minimal risk information sheet.
To fill out a minimal risk information sheet, the researcher must provide details on the study protocol, potential risks, participant eligibility criteria, and safety measures.
The purpose of a minimal risk information sheet is to ensure that participants are fully informed about low-risk studies and to minimize potential harm or danger.
Information such as study protocol, risks and benefits, participant eligibility criteria, and safety measures must be reported on a minimal risk information sheet.
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