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Clinically extremely vulnerable people If your doctor or GP has classed you as clinically extremely vulnerable because they think you\'re at high risk of getting seriously ill you\'ve been identified
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How to fill out additional info to consent

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Start by reviewing the consent form to see if there is any additional information required.
02
Provide all the relevant details and answer any specific questions asked in the additional info section of the form.
03
If the additional info section is not included in the consent form, contact the person or organization responsible for the form to clarify if any additional information is needed.
04
Fill out the additional info accurately and honestly.
05
Double-check your answers to ensure they are complete and consistent with the rest of the information provided.
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Finally, submit the consent form with the additional info filled out.

Who needs additional info to consent?

01
Anyone who is required to provide additional information as specified in the consent form.
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Additional info to consent is any supplementary information required to be provided along with the main consent form.
Anyone seeking consent for a particular action or decision may be required to file additional info to consent, depending on the specific requirements of the situation.
Additional info to consent should be filled out by providing all requested information in the designated sections or accompanying documents as per the instructions provided.
The purpose of additional info to consent is to provide more detailed information or clarification to ensure that the individual giving consent fully understands the implications of their decision.
The information required on additional info to consent can vary depending on the nature of the consent being sought, but typically includes relevant details about the action or decision, potential risks and benefits, alternatives, and contact information for further questions.
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