Welcome to Your Portal for Regulatory Information!
This interactive, up-to-date, freely-accessible repository of regulatory resources is a comprehensive web portal where anyone can easily access information from government, academic, and scientific institutions, with the goal of providing the clinical research workforce with regulatory information to plan and conduct clinical trials and bring their bench discoveries to the patient's bedside.
Not sure where to begin? Watch the OpenRegSource tour video, or start with this page.
![Welcome to the Regulatory Repository of Resources!](https://sc-ctsi.org/uploads/resources/Front-page-collage-copy.jpg)
Interested in studying Regulatory Science?
Visit the USC Mann Department of Regulatory and Quality Sciences or enroll in our free Clinical Trial Quality Training Series courses. Learn more about the self-paced series HERE.
Created and maintained by the Southern California Clinical and Translational Institute (SC CTSI) Regulatory and Knowledge and Support (RKS) core, this work is supported by grants UL1TR001855 from the National Center for Advancing Translational Science (NCATS) of the U.S. National Institutes of Health. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.
The contents of this Regulatory Repository ©2024 USC Mann School of Pharmacy and Pharmaceutical Sciences Department of Regulatory and Quality Sciences.
Table of Contents
- What is my medical product?
- What stage am I in the product development process?
- Clinical Research
- Patenting
- Manufacturing
- Regulatory Paths to Market
- Glossary of Terms used in Regulatory Science