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DEPARTMENT OF HEALTH AND HUMAN SERVICES PUBLIC HEALTH SERVICE FOOD AND DRUG ADMINISTRATION STATEMENT OF INVESTIGATOR (TITLE 21, CODE OF FEDERAL REGULATIONS (CFR) PART 312) (See instructions on reverse
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How to fill out investigator-statement- form- fda- 1572

01
To fill out the investigator-statement- form- fda- 1572, follow these steps:
02
Download the investigator-statement- form- fda- 1572 from the FDA's official website.
03
Read the instructions provided with the form carefully.
04
Fill in your name, address, and contact information in the designated fields.
05
Provide detailed information about the study you are conducting, including the title, protocol number, and purpose.
06
Indicate the name and address of the medical institution where the study will be conducted.
07
Sign and date the form to certify that the information provided is accurate and complete.
08
Make a copy of the completed form for your records.
09
Submit the original form to the FDA as requested or in accordance with the guidelines provided.

Who needs investigator-statement- form- fda- 1572?

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The investigator-statement- form- fda- 1572 is required by individuals who are conducting clinical studies or trials that involve the use of investigational drugs, biologics, or devices in the United States.
02
This form is typically filled out by principal investigators or study sponsors who are responsible for overseeing the study and ensuring compliance with FDA regulations.

What is Investigator-Statement- - FDA- 1572 - Centers for ... Form?

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The FDA Form 1572, also known as the Investigator Statement, is a document that clinical investigators must complete and submit to the FDA. It provides information about the investigator and the site where the clinical trials will be conducted.
Clinical investigators who conduct clinical trials of investigational drugs on behalf of sponsors are required to file Form FDA 1572.
To fill out Form FDA 1572, investigators must enter their personal and professional information, including qualifications, details about the clinical site, and the protocol number of the study. It should be completed accurately and signed.
The purpose of Form FDA 1572 is to provide the FDA with essential information about the investigator conducting the clinical trial, ensuring compliance with regulations and safety standards in clinical research.
The form requires details such as the investigator's name, address, qualifications, sites where research will be conducted, and the names of the research staff. It also includes information about the study protocol.
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