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Version 2 15/03/2011 Reference Range Project Center Number: Study Number: Patient Identification Number for this trial: CONSENT FORM Title of Project: Name of Researcher: Please initial box 1. I confirm
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01
Begin by carefully reading each section of the consent form. Make sure you understand the purpose and significance of each section before proceeding.
02
Provide your personal information accurately and legibly. This may include your name, address, contact information, and any other requested details.
03
Follow any instructions or guidelines provided in the form. These could include marking checkboxes, filling in blanks, or providing additional information in the designated spaces.
04
If there are any sections or terms that you are unsure about, don't hesitate to seek clarification. Contact the relevant authority or organization responsible for the form and ask for assistance in understanding any confusing elements.
05
Review your filled form for any mistakes or omissions. Double-check your entries to ensure accuracy and completeness.
06
If required, obtain any necessary signatures. This could be your own signature or that of a guardian or representative if applicable. Follow the specified method for signing the consent form (e.g., handwritten or digital).
07
Make a copy of the filled consent form for your records. It's always a good idea to have a backup in case the original gets misplaced or if you need to refer back to it in the future.
Who needs consent form version 3?
01
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02
Organizations or agencies that are responsible for conducting or overseeing the activity or event may require participants to complete this particular version of the consent form.
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Specific situations or circumstances may dictate the need for consent form version 3. It could be based on legal requirements, specific changes in regulations, or updated policies that necessitate the use of this particular form version.
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