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APPENDIX 8B: ASSENT AGE 12 17 YEARS Investigational New Drug (IND) BB 11184 IRB # 4167 Protocol #4167 BB IND 11184 ASSENT FOR ADDITIONAL BLOOD DRAWS WITH THE USE OF DIPHTHERIA ANTITOXIN (DAT) FOR
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Step 1: Start by downloading the Appendix-8B-Assent form from a reliable source.
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Step 2: Read the instructions carefully to understand the requirements and purpose of the form.
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Step 3: Fill in the personal details of the individual providing assent, such as their name, age, address, and contact information.
04
Step 4: Provide information about the investigational study, including its purpose, procedures, potential risks and benefits, and any compensation offered.
05
Step 5: Make sure to include any additional information or comments required by the form.
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Step 6: Review the filled-out form for any errors or missing information.
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Step 8: Submit the completed Appendix-8B-Assent form to the appropriate authority or organization as specified in the instructions.

Who needs appendix-8b-assent 12-17 years investigational?

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Appendix-8B-Assent 12-17 years investigational is required for individuals between the ages of 12 and 17 who are participating in an investigational study.
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Appendix-8b-assent 12-17 years investigational is a form that must be filled out when conducting investigational studies with participants aged 12-17 years old.
Researchers and organizations conducting investigational studies with participants aged 12-17 years old are required to file appendix-8b-assent.
To fill out appendix-8b-assent, researchers need to provide detailed information about the study, risks involved, benefits, and ensure that the assent process is properly conducted.
The purpose of appendix-8b-assent is to ensure that minors involved in investigational studies understand the study, risks, and benefits, and give their assent to participate.
Information such as study details, risks involved, benefits, how assent was obtained, and any additional information required by the regulatory body must be reported on appendix-8b-assent.
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