The rapidly expanding pharmaceutical and biomedical industries necessitate a greater number of Regulatory Affairs professionals to manage the FDA approval process of new products and maintain regulatory compliance. Specialized and convenient education is crucial for busy professionals to gain an understanding of the scientific and technical background of new products. The program plan is ideal for working professionals and consists of three graduate paths, a certificate in BioPharma Regulatory Affairs (14 semester hours), a certificate in Clinical Trials Design and Management (17 semester hours), and, if the student completes additional course work, a Master’s of Science Degree with an emphasis in Regulatory Affairs. Each is delivered by Internet-based instruction, with occasional live sessions on the UGA Gwinnett Campus. Affairs. UGA’s educational program and degree option for Regulatory Affairs professionals covers: Pharmaceuticals, Biologics, Medical Devices, Veterinary Products, and Combination Products. For additional information, please visit our website.