This graduate certificate program is designed for individuals with backgrounds in biological, pharmaceutical, biomedical sciences, or biomedical engineering who want to specialize in ensuring the quality of medical products. It covers the regulations and guidelines critical for maintaining the quality of drugs, biologics, and medical devices in both the United States and internationally. The program provides a foundational understanding of quality practices and systems, preparing specialists for high-demand roles in the regulatory and quality science fields.
Graduates are prepared for a wide array of roles within the regulatory and quality sciences, including positions with the FDA and the broader industry. The skills acquired are applicable across diverse sectors of medical product development and oversight.
The program is structured for working professionals, allowing students to take one or two courses per term.
The program requires 12 units. Specific fee structures should be confirmed with the university.
Accredited graduate certificates.
A Bachelor's degree in biological, pharmaceutical, biomedical sciences, or biomedical engineering is required. The program is structured for working professionals and allows for flexible course loads.
The program requires the satisfactory completion of 12 units beyond the baccalaureate degree.
International tuition rates must be confirmed directly with the university.
Graduates are prepared for roles in regulatory and quality sciences, including positions with the FDA and in various industry sectors related to medical product development and oversight.
Yes, courses can typically be taken either in-person or online. Online students participate in the same classes as onsite students, with lectures available in real-time or on-demand.
The application deadline for a Fall start is June 6th.