M.S. in Drug Regulatory Affairs

M.S. in Drug Regulatory Affairs

Master degree
24 months
Application deadlines: 30/04/2019
Processing time: 60 days
Application fee: $49
Intakes: August 2019

Program overview

The mission of the Master of Science program in Drug Regulatory Affairs is to prepare students to become lifelong learners and leaders in a variety of settings including biotechnology, medical devices, pharmaceuticals, consulting arena, and liaise with government and regulatory agencies worldwide. Students will: a) Demonstrate a mastery of a broad didactic foundation in regulatory affairs gained in advanced coursework; b) Develop strong skills through exposure to significant regulatory projects and case studies during which they translate their knowledge into practice; and c) Utilize professional skills such as statistical analysis, knowledge of regulatory guidance documents, as well as written and verbal communication skills. These abilities will be acquired through specific coursework and seminars and other professional and personal development offered during the course of study.

Study options

Study options
This program can be done
On campus



Undergrad transcripts Statement of purpose 2 letters of recommendation Resume TOEFL/IELTS score

Career opportunities

Employment opportunities include: Collecting data and preparing submissions to regulatory agencies Assisting in the development of procedures to ensure regulatory compliance Interfacing with regulatory agencies Facilitating identification and resolution of scientific and regulatory issues with regulatory agencies Remaining current with federal and international regulations and communicating that information within the organization, including the creation of training materials Participating in the development of new products and services Participating in quality audits

Campus location

New York , United States

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