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Annex 7.1: Informed Consent Form for In Depth Interview Protocol No.17086Version No. 1.00Date: 28082017Protocol Title: Perceptions and experiences on implementing technology (DHIS2 software) to collect

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How to fill out annex 71 informed consent

01

Review the contents of annex 71 informed consent form.

02

Fill out the patient's name, date of birth, and any other required personal information.

03

Specify the purpose of the informed consent and the procedures involved.

04

Provide information on the risks and benefits of the procedure.

05

Make sure the patient or legal guardian signs and dates the form.

06

Retain a copy of the fully completed form for your records.

Who needs annex 71 informed consent?

01

Any individual who is involved in a medical procedure or study that requires informed consent.

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What is annex 71 informed consent?

Annex 71 informed consent is a document required by regulations that outlines permission from individuals to participate in a specific activity or study.

Who is required to file annex 71 informed consent?

Researchers, institutions, or organizations conducting studies or activities that involve human participants are required to file annex 71 informed consent.

How to fill out annex 71 informed consent?

Annex 71 informed consent should be filled out by providing all necessary information about the study or activity, obtaining signatures from participants or their legal guardians, and following any specific instructions mandated by regulations.

What is the purpose of annex 71 informed consent?

The purpose of annex 71 informed consent is to ensure that participants are fully informed about the study or activity, understand the risks and benefits, and voluntarily agree to participate.

What information must be reported on annex 71 informed consent?

Information such as the purpose of the study, risks involved, benefits, confidentiality measures, contact information for questions or concerns, and any other relevant details must be reported on annex 71 informed consent.

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