UGA BioPharma Program Descriptions
(All Programs are online and part-time)
Due to the rapidly expanding pharmaceutical and biomedical industries, an increase in the number of Regulatory Affairs professionals is needed to get approval for new products and maintain compliance with regulatory policies and procedures. Specialized and convenient education is crucial for busy professionals to gain and sustain an understanding of the ever-changing regulatory environment. This program is also appropriate for individuals with a background in the industry who wish to enter the 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. 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