Form FDA 1572 Essentials: Updated for ICH E6(R3)​

Form FDA 1572 doesn’t have to be complicated. This practical training course equips sponsor personnel and site staff with the knowledge and tools to complete the Statement of Investigator accurately and confidently—right from the start.

Whether you’re guiding sites, completing the form, or reviewing submissions, this course breaks down the why, when, and how of Form FDA 1572 to streamline workflows and reduce regulatory risk. Updated to reflect the latest ICH E6(R3) guidelines, the course includes job aids like completion tips, decision trees, FAQs, and hands-on exercises to make compliance easier for everyone involved.

Upon completion of this training program, participants should be able to:

• ​​Summarize the description and purpose of Form FDA 1572 as presented in the Form FDA 1572 Introduction section. 

• ​Evaluate the necessity for completing Form FDA 1572 as presented in the Application and Requirements section. 

• ​Determine which documents are required to support the information included on Form FDA 1572 as presented in the Documentation and Expectations section.   ​ 

This course will assist clinical research professionals involved in reviewing and/or completing the Form FDA 1572 build competency in Clinical Trials Operations (GCPs), Medicines Development and Regulation, and Study and Site Management. Explore Competencies >

Approved for 1.5 ACRP Contact Hours | Available 1 Year from Enrollment Date