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Consent in online surrender ICT Project Coordinator We would like to ask you to participate in the data collection for the European Research Project ERICA (Ethical Issues of Emerging ICT Applications).
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How to fill out consent in online survey

01
Read the instructions provided with the online survey.
02
Locate the consent form within the survey.
03
Begin filling out the consent form by entering your personal information such as name, age, and contact details.
04
Carefully read the terms and conditions of the survey and make sure you understand them.
05
Tick the box or provide your electronic signature to indicate your consent.
06
If there are any additional questions or sections in the consent form, answer them as required.
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Double-check all the information you have entered for accuracy.
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Once you are confident that the consent form is complete and accurate, submit it as directed by the online survey platform.
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Keep a copy of the consent form for your records, if necessary.

Who needs consent in online survey?

01
Anyone participating in an online survey usually needs to provide consent.
02
This may include individuals of legal age, minors (with parental or guardian consent), or specific target groups for which the survey is intended.
03
Online surveys often require consent to ensure ethical and legal compliance in collecting and analyzing data.

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Consent in online survey is the agreement given by participants to voluntarily participate in the survey after being informed of the purpose and risks involved.
Researchers or organizations conducting the online survey are required to file consent from the participants.
Consent in online survey can be filled out by providing clear and concise information about the study, risks involved, and obtaining participant signatures either electronically or in-person.
The purpose of consent in online survey is to ensure that participants are fully informed of the survey, its purpose, risks involved, and voluntarily agree to participate.
The consent form in online survey must include information about the study purpose, risks involved, participant rights, confidentiality, and contact information of the researchers.
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