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FDA has published an Information Sheet for Guidance for Sponsors, Clinical Investigators, and IRBs Frequently Asked Questions – Statement of Investigator (Form FDA 1572) May 2010 that is intended to assist sponsors, clinical investigators, and institutional review boards involved in clinical investigations of sign the 1572 when the investigator knows he/she cannot commit to all of the Guidance, would the non-US investigators also be in compliance with FDA's. 5 May 2011 Information Sheet Guidance for Sponsors, Clinical Investigators, and IRBs Asked Questions - Statement of Investigator (Form FDA 1572 STATEMENT OF INVESTIGATOR. (TITLE 21, CODE OF FEDERAL REGULATIONS (CFR) PART 312). (See instructions on reverse side.) Form Approved: OMB 1 Jul 2018 There has previously been no alternative non-U.S. regulator?s statement available; therefore, the instructions on the FDA 1572 form itself and Statement of Investigator, Form FDA 1572 What is the FDA Form 1572? . questions and/or better instructions for completing the 1572 FDA regulations use The Statement of Investigator, Form FDA 1572, is an agreement, signed by the Guidance for Sponsors, Clinical Investigators, and IRBs Frequently Asked Guidance on FDA Form 1572 Statement of Investigator in aclinical trial.Information Sheet Guidance for Sponsors, Clinical Investigators, and IRBs. Frequently Asked Questions – Statement of Investigator (Form FDA 1572) Guidance form for FDA Form 1572 v 2.0: September 8, 2014. Page 1 of The Statement of Investigator, Form FDA 1572, is an agreement signed by the principal