Informed Consent form template

The primary purposes of an Informed Consent form are to ensure that participants are fully educated about the scope, procedures, risks, and benefits of a given activity and that they consciously agree to participate. This is particularly relevant in the field of medicine, research, and clinical trials, where the potential risk to participants needs to be communicated transparently.

The informed consent form

Please fill in the following details to proceed

Expert Tips

Expert Tips for Creating Effective Informed Consent

Get better responses for your the informed consent form with these tips

1
Clarity of Language

Use simple and clear language to ensure all participants understand the contents of the form.

2
Detailed Information

Include all details about the purpose, procedures, risks, and benefits of the activity.

3
Voluntary Participation

Highlight that participation is voluntary and that the participant can withdraw at any time.

4
Privacy Assurance

Ensure to mention how the data will be used, stored, and protected.

5
Contact Information

Provide contact information for participants to make inquiries or express concerns.

6
Signature and Date

Include a section for signature and date to confirm the participant’s consent.

7
Follow Legal Guidelines

Ensure your form complies with all relevant local and international laws and guidelines.

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