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Informed Consent Form Template for Consent for Storage and Future Use of Unused Human Biological Material (HBM)Notes to Applicants: 1. Please note that this is a template developed by the WHO ERC. It
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How to fill out informed consent form template

01
To fill out an informed consent form template, follow these steps:
02
Begin by reading the entire form to understand its purpose and what information is required.
03
Fill in your personal details such as your name, address, contact information, and date of birth.
04
Provide information about the research study or medical procedure for which you are giving consent.
05
Carefully read and understand each section of the form, including any risks or side effects that may be involved.
06
If you have any questions or concerns, don't hesitate to ask the investigator or medical professional before signing the form.
07
Sign and date the form to indicate your consent.
08
If required, have a witness also sign the form to verify that you have willingly provided your informed consent.
09
Make a copy of the signed form for your own records, if necessary.
10
Submit the completed form to the appropriate person or organization as instructed.

Who needs informed consent form template?

01
Various individuals and entities may require an informed consent form template, including:
02
- Researchers conducting scientific studies or clinical trials
03
- Healthcare providers performing medical procedures or surgeries
04
- Institutional review boards overseeing research involving human subjects
05
- Pharmaceutical companies testing new drugs or therapies
06
- Educational institutions conducting research on students
07
- Government agencies conducting studies or collecting data
08
- Legal entities requiring informed consent for certain activities
09
- Any situation where it is necessary to ensure that individuals have given their voluntary and informed consent
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The informed consent form template is a document that outlines the details of a study or procedure, including the risks and benefits, that a participant must read and sign before participating.
Researchers, medical professionals, and institutions conducting studies or procedures are required to file an informed consent form template.
The informed consent form template should be filled out by providing all necessary information, explaining the study or procedure in detail, and ensuring that the participant understands and agrees to the terms.
The purpose of the informed consent form template is to ensure that participants are fully informed about a study or procedure before agreeing to participate, and to protect their rights and well-being.
The informed consent form template must include the purpose of the study or procedure, the risks and benefits involved, the participant's rights, confidentiality measures, and contact information for questions or concerns.
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