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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 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
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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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What is appendix-8b-assent 12-17 years investigational?
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.
Who is required to file appendix-8b-assent 12-17 years investigational?
Researchers and organizations conducting investigational studies with participants aged 12-17 years old are required to file appendix-8b-assent.
How to fill out appendix-8b-assent 12-17 years investigational?
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.
What is the purpose of appendix-8b-assent 12-17 years investigational?
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.
What information must be reported on appendix-8b-assent 12-17 years investigational?
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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