The Association of Clinical Research Professionals

Form FDA 1572: Get it Right the First Time

The Statement of Investigator (Form FDA 1572) doesn’t have to be complicated. This training program helps you get it right the first time.

Ideal for sponsor personnel instructing sites on completion, site staff completing the form and sponsor personnel reviewing it, this course answers the questions of why, when and how to complete the FDA 1572 to make everyone’s jobs easier.

Ease the regulatory burden of handling the FDA 1572 by leveraging the course’s job aides, including completion tips, decision trees, FAQs, and practice exercises.

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

  • Describe the scope and purpose of Form 1572.
  • Evaluate the application and requirements for completing Form 1572.
  • Determine which documents are required to support the information included in Form 1572.

This courses helps clinical research professionals involved in completing and/or reviewing 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