Get the Form 1572 in Clinical Research - Free Ebooks PDF & Documents

Save As... Print Export Data Import Data Next Page E-mail Form Reset Form Approved: OMB No. 0910-0014. Expiration Date: January 31, 2006. See OMB Statement on Reverse. DEPARTMENT OF HEALTH AND HUMAN

How to fill out form 1572 in clinical

How to fill out form 1572 in clinical?

1. The first step is to carefully review the form instructions provided by the relevant regulatory authority, such as the Food and Drug Administration (FDA) in the United States.
2. Begin by completing the header of the form, which includes the trial title, protocol number, investigational site information, and the date of completion.
3. Next, provide details about the investigator, including their name, address, telephone number, and qualifications in the specific therapeutic area.
4. Fill in information regarding the delegation of trial-related duties and responsibilities to clinical research staff members involved in the study. Include their names, qualifications, and the functions they will perform.
5. List all the sub-investigators who will be assisting the principal investigator and provide their credentials and responsibilities.
6. Include information about the facility where the clinical trial will be conducted, such as the name, address, and contact details.
7. Indicate whether the investigator or any sub-investigator has any financial interests or arrangements with the sponsor or any other conflicting interests that may affect the trial's integrity.
8. Sign and date the form to certify the accuracy and completeness of the information provided. Include the name and title of the signatory.

Who needs form 1572 in clinical?

1. Investigators or principal investigators conducting clinical trials need to fill out form 1572. This form is required by regulatory authorities to ensure the qualifications, responsibilities, and commitments of the investigators involved in the study.
2. Sponsors of the clinical trial also require form 1572 to document and verify the investigators' compliance with the trial protocol and ensure the safety and ethical conduct of the trial.
3. Regulatory authorities, such as the FDA, may request form 1572 during the review process to assess the appropriateness and qualification of the investigators and site involved in a clinical trial.

For pdfFiller’s FAQs

What is form 1572 in clinical?

Form 1572 is a document used in clinical trials to capture key information about an investigator's qualifications, financial interests, and commitments.

Who is required to file form 1572 in clinical?

Investigators or sponsors of clinical trials are required to file form 1572.

How to fill out form 1572 in clinical?

To fill out form 1572, one needs to provide information such as investigator's name, contact details, qualifications, financial interests, and commitments.

What is the purpose of form 1572 in clinical?

The purpose of form 1572 is to ensure that investigators conducting clinical trials are qualified and have no conflicting interests that could bias the study results.

What information must be reported on form 1572 in clinical?

Form 1572 requires the reporting of investigator's personal information, professional qualifications, financial interests, and commitments.

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