Get the free fda 1572 template

Collection of this information is authorized under 21 CFR 312.53. The primary use is to identify qualified investigators and as experts to participate in clinical investigations at the National Cancer

How to fill out fda 1572 template form

How to fill out FDA Form 1572:

1. Begin by downloading a copy of FDA Form 1572 from the official FDA website or obtain it from a reliable source.
2. Carefully read through the instructions provided on the form to familiarize yourself with the requirements and guidelines.
3. Fill in the requested general information, such as the study title, protocol number, and date of completion.
4. Provide details about the investigator, including their name, address, phone number, and professional qualifications.
5. Indicate whether the investigator will be using an institution or facility for the study and provide the necessary details if applicable.
6. Answer the questions regarding the financial disclosures by the investigator and the institution or facility involved.
7. In the "Agreement" section, sign and date the form to confirm your commitment and compliance with the FDA regulations and guidelines.
8. Ensure all required supporting documents, such as curriculum vitae and medical licenses, are attached with Form 1572.
9. Double-check all the entered information for accuracy and completeness before submitting the form.

Who needs FDA Form 1572?

1. Clinical investigators conducting drug trials regulated by the FDA.
2. Sponsors or sponsors-investigators overseeing clinical investigations.
3. Institutions or facilities used for clinical studies, if applicable.

Note: FDA Form 1572 is necessary to establish the credentials and commitment of the clinical investigators and sponsors involved in FDA-regulated clinical trials.

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What is fda form 1572?

FDA Form 1572 is a document used to provide information about the clinical trial conduct, including details about the investigator, the site of the trial, and the study protocol.

Who is required to file fda form 1572?

Clinical investigators who are conducting studies regulated by the FDA under an Investigational New Drug (IND) application must file FDA Form 1572.

How to fill out fda form 1572?

To fill out FDA Form 1572, you need to provide the investigator's name, address, qualifications, the title of the study, and information about the institution and the subject population.

What is the purpose of fda form 1572?

The purpose of FDA Form 1572 is to ensure that investigators have the appropriate qualifications and resources to conduct the clinical study, as well as to collect key information about the trial.

What information must be reported on fda form 1572?

FDA Form 1572 must report the investigator's name and address, the protocol title, the clinical study's objectives, and details about any financial arrangements, as well as a list of study staff.