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X118225_NHS_NUTH29_p5_gs_x118225_NHS_NUTH29_p5_gs 27/02/2013 12:05 Page 1Consent Form 3 For Patients with capacity Patient/Person with parental responsibility Agreement to Investigation or Treatment
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01
Fill out the personal information section including name, address, and contact information.
02
Provide detailed information about the purpose of the consent form and any relevant background information.
03
Clearly outline the scope of the consent and any limitations or restrictions that apply.
04
Ensure that all parties involved sign and date the form to indicate their agreement.
05
Make copies of the completed form for all parties involved and keep a copy for your records.

Who needs consent form 3 for?

01
Consent Form 3 is typically required for individuals who are participating in a research study, clinical trial, or any other situation where informed consent is necessary.
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Consent form 3 is used to obtain permission from a participant or individual before collecting or using their personal information.
Any organization or individual that collects or uses personal information from a participant or individual is required to file consent form 3.
Consent form 3 should be filled out with the participant's or individual's personal information, details on the purpose of data collection, and a clear statement of consent.
The purpose of consent form 3 is to ensure that individuals are aware of and agree to the collection and use of their personal information.
Information such as the individual's name, contact details, purpose of data collection, and a section for the individual to provide their consent must be reported on consent form 3.
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