UGA BioPharma Programs (All programs are ONLINE and PART-TIME.)
The rapid expansion of pharmaceutical and biomedical products requires a greater number of highly skilled Regulatory Affairs Professionals to oversee the approval for new product lines and manage compliance with complex regulatory policies and procedures. Specialized and convenient education is crucial for busy professionals to develop and sustain an understanding of the ever-changing regulatory environment. The Masters of Science in Regulatory Affairs Program assures a strong professional background needed to succeed in administrative positions and specialized areas required of this hands-on profession. Learn More >>
Due to the rapidly expanding biomedical industries, an increase in the number of Regulatory Affairs professionals is needed to maintain compliance with regulatory policies and procedures for multiple product lines. The Regulatory Affairs Graduate Certificate Program provides a foundational core for individuals who wish to round out their experiences in regulatory affairs or transition into entry-level regulatory affairs positions. Specialized and convenient education is crucial for these busy professionals to maintain an understanding of the scientific and technical background of new products. Learn More >>
Geared toward a wide range of professionals, the Clinical Trials Design and Management Certificate Program provides a solid foundation in the effective design, management and monitoring of clinical trials. Moreover, the interdisciplinary program encompasses biostatistics, regulations, project management and bioethics in the context of drug and device testing and commercialization. Learn More >>
After only completing two classes, I have already implemented the knowledge I have gained in my job. I am taking this program to prepare to take the RAC accreditation with RAPS and I have no doubt that I will do well because of the knowledge I gained."
– April L. Carroll Associate Manager, Regulatory Affairs Merial