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Form Approved: OMB No. 09100014 Expiration Date: March 31, 2022, See OMB Statement on Reverse. DEPARTMENT OF HEALTH AND HUMAN SERVICES FOOD AND DRUG ADMINISTRATIONSTATEMENT OF INVESTIGATOR (TITLE
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How to fill out form fda 1572
How to fill out form fda 1572
01
To fill out form FDA 1572, follow these steps:
02
Start by providing your name and contact information at the top of the form.
03
In section 1, indicate the title of the study and the name of the sponsor.
04
Fill in section 2 by providing the names and addresses of the investigators involved in the study.
05
In section 3, provide information about the research site, including the name, address, and phone number.
06
Section 4 requires the signature and date of the investigator conducting the study.
07
If you are the sponsor, complete section 5 by providing your name, address, and phone number.
08
Finally, review the completed form for accuracy and ensure all necessary signatures are included.
Who needs form fda 1572?
01
Form FDA 1572 is needed by investigators who are conducting clinical trials or studies that involve investigational drugs or biologics. It is also required by sponsors or sponsors-investigators who are initiating such studies.
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What is form fda 1572?
Form FDA 1572 is an FDA form that is used for the purpose of providing information about the clinical investigator involved in a clinical study.
Who is required to file form fda 1572?
The clinical investigator who is participating in a clinical study is required to file form FDA 1572.
How to fill out form fda 1572?
Form FDA 1572 can be filled out by providing the required information about the clinical investigator, including contact information, qualifications, and the specific study being conducted.
What is the purpose of form fda 1572?
The purpose of form FDA 1572 is to document the agreement of the clinical investigator to conduct the study in accordance with FDA regulations.
What information must be reported on form fda 1572?
The information that must be reported on form FDA 1572 includes the name and address of the clinical investigator, the research protocol title, and the drug being studied.
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