ReGARDD provides academic researchers with the regulatory tools and resources necessary to successfully navigate the pathway from discovery to clinical implementation of new drugs, biologics, and medical devices.
(ReGARDD) provides academic researchers with the regulatory tools and resources necessary to successfully navigate the pathway from discovery to clinical implementation of new drugs, biologics, and medical devices.
Combining the regulatory talents from regional CTSA hubs and the Research Triangle Park (RTP), our focus is to move promising products and novel discoveries into clinical trials. It’s partners are UNC-Chapel Hill, Duke, the Medical University of South Carolina, Wake Forest, and RTI International.
Use ReGARDD for:
- INDs – preparation and maintenance
- IDEs – preparation and maintenance
- Educational Videos
- Access to workshops, presentations and forums
- Access to CTSA Institution Training Resources
To learn more about ReGARDD and to access helpful tools and resources, visit this website.