Pharmaceutical Analysis with Regulatory Affairs Kingston University

Overview

The Pharmaceutical Analysis with Regulatory Affairs programme offered by Kingston University involves overseeing the process from drug development and clinical trials to manufacturing, marketing, along with post-market monitoring to protect public health. From drug formulation, to quality control and regulatory affairs, you'll gain hands-on experience in industry-standard labs. Learn from experts shaping the future of healthcare.

Key Facts

Kingston University's MSc in Pharmaceutical Analysis with Regulatory Affairs provides the expertise needed to drive advances in drug development, formulation and safety. Regulatory affairs is a popular career choice due to the increasing need for safe products and the expansion of global regulations. Whether you aspire to work in the pharmaceutical industry, regulatory bodies or research, this course opens doors to a wealth of career opportunities. You’ll work with cutting-edge technologies and gain work experience that will give you a competitive edge in the global pharmaceutical sector.

With a focus on emerging trends in drug safety, pharmaceutical technology, and regulatory frameworks, this course equips you to make a significant impact in the global pharmaceutical industry.

Career opportunities

Whether you aim to work in research, production or regulatory roles, the MSc Pharmaceutical Analysis with Regulatory Affairs will open doors to diverse, rewarding career paths. The course will prepare you for roles in governmental regulatory agencies such as the Medicines and Healthcare products Regulatory Agency (MHRA). The Organisation of Professionals in regulatory Affairs estimates that around 35% of all industrial pharmacy roles are directly related to regulatory affairs.