Program Information
Degree Offered
MS
Format: Campus, Online
Program Description:
The Master of Science in Regulatory Affairs for Drugs, Biologics, and Medical Devices is designed to educate and prepare RA professionals who will play a pivotal role in ensuring compliance with applicable laws and regulations in the development and commercialization of the healthcare products of their company. While this program can be an excellent complement to those with health- or science-related degrees, there are many rewarding career opportunities with regulatory affairs for individuals with a variety of backgrounds.
Program Objectives:
-Gain the essential knowledge and skills required to help companies navigate an increasingly complex regulatory environment
-Acquire the foundation necessary to work within a variety of fields, including medical product development, pharmaceutical sales, strategic marketing, and clinical investigations
-Examine every step of the drug development and regulation process
-Sharpen your understanding of the laws that govern the development, manufacturing, and commercial distribution of drugs, biologics, and medical devices
-Analyze how emerging developments and trends are reshaping medical device regulations
Accreditation:
NEASC
Tuition & Financial Aid
Financial Aid Offered: No
Classification: Doctoral/Research Universities - Extensive
Institution Sector: Private not-for-profit
Locale: Large City
Size & Settings: 20,000 and above