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Appendix B: Consent forms Participant identification number where applicable CONSENT FORM Project Title: BLASTER Name of Researcher: I confirm that I have read and understood the information sheet
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How to fill out consent form pi sheet

01
Begin by reading the consent form and all accompanying instructions.
02
Provide your personal information accurately and completely as requested.
03
Ensure that all sections and fields are completed as required.
04
Read and understand the purpose and nature of the study or activity that the consent form is related to.
05
Carefully consider the potential risks and benefits of participation.
06
Seek clarification or additional information from the responsible party if needed.
07
Sign and date the consent form to show your agreement and understanding.
08
Return the completed form to the appropriate person or organization as instructed.

Who needs consent form pi sheet?

01
Anyone who is willing to participate in a study or activity that requires informed consent.
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A consent form PI sheet is a document used in research and clinical trials to obtain and record participants' consent for the use of their personal information in the study.
Researchers and organizations conducting clinical trials or studies involving human subjects are required to file the consent form PI sheet.
To fill out the consent form PI sheet, researchers should provide clear information about the study, including its purpose, procedures, risks, benefits, and confidentiality measures. Participants must sign to indicate their understanding and agreement.
The purpose of the consent form PI sheet is to ensure that participants are fully informed about the study and voluntarily agree to participate, thereby protecting their rights and welfare.
The consent form PI sheet must include details about the study's purpose, procedures, risks, benefits, confidentiality measures, and contact information for questions, as well as a statement of voluntary participation.
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