Program Highlights: ; Two program tracks: Biopharmaceutical and Medical Devices ; Part-time program options available for working professionals. ; Located near biomedical, biotech and pharmaceutical companies and other job opportunities in Irvine, California. ; Program covers the steps required to bring a medical product to market, both in the U.S. and around the globe.
Advance your career in regulatory science with online masters & certificate courses for professionals in drug & medical device development, pharmaceutical research, clinical trials, etc.
Online : Location, Full-Time Part-Time : Commitment, 12-18 months : Duration of Program, Fall, Spring, Winter : Entry Terms, No : Meets F1 Visa Requirements
a 입학을 위한 자격요건 및 학비, 입학학기를 알아보세요 Master of Science in Regulatory Affairs at San Diego State University in United States
Our programs prepare students for careers in three broad areas: The versatility of many of our degrees allows KGI graduates to work in a variety of settings. Exposure to the biotech and pharmaceutical industries is woven throughout all of our programs, giving students a unique exposure to opportunities. We encourage you to learn more about all of our programs, discovering new passions that will take you into leadership roles within the biotech or healthcare industries. If you have questions about any programs, please contact the admissions team ...
Program Overview ; As a regulatory affairs or clinical research professional, you will lead and play a significant role in the development and advancement of medical products for some of the biggest companies and agencies in the country and worldwide. You will engage in the design, manufacturing, and testing of products to make sure they comply with the regulations and standards of the industry. The regulatory and clinical research management (RCRM) graduate program is designed for individuals who wish to start or advance a career in the regula ...
The University of Washington’s Master of Science in Biomedical Regulatory Affairs trains professionals to effectively manage the process of bringing new medical products to market. In this two-year...
The biomedical industry has grown rapidly, and this has fueled a large — and largely unmet — demand for regulatory professionals, both nationally and internationally. The USC Master’s in Regulatory...
배울 내용 ; How to create a registration dossier ; How to provide a qualified assessment of clinical documents ; How to develop an understanding of language fundamentals and style-guide conventions ; How to increase your salary
Director of Regulatory Affairs - Software & Systems Job Description The Director of Regulatory Affairs-Software & Systems will play a critical role in ensuring Philips Software driven...