In collaboration with the European University, discover the complete master’s degree with which to specialise in the industry.
The Master’s in Pharmaceutical and Biotechnological Industry is an advanced program designed to train students in the core competencies required in the pharmaceutical sector. This continuing education master’s program covers everything from drug development to applied biotechnology in healthcare, preparing students to face the technological and regulatory challenges of pharmaceutical laboratories and biotech companies.
The objective of the program is for you to gain an in-depth understanding of the regulations governing biotechnological products and to comprehend the entire process—from the initial development of an idea to its commercialization.
You will learn about the structure of the biotechnology industry at both national and global levels, key concepts in biology, cellular pathology, and regenerative medicine, as well as familiarize yourself with health technologies such as robotics and artificial intelligence.
You will acquire knowledge of the preclinical regulatory environment, principles of Good Laboratory Practices (GLP), and the design of experimental models, all with an ethical and risk-based approach.
You will specialize in Good Manufacturing Practices (GMP), biosafety, and the production of biological products, advanced therapies, and medical devices, including medical software tools.
You will study the regulation of clinical trials, including their ethical and legal aspects, and become familiar with the design, monitoring, and statistical analysis of these studies in both pharmaceutical and medical products.
You will understand how regulatory agencies such as EMA, AEMPS, and the FDA operate, and study the registration process for drugs and medical devices, including advanced therapies and orphan drugs.
You will be trained in market access strategies for pharmaceutical and medical products, including pricing, funding, health economics evaluation, and commercial strategies.
You will develop skills to identify and report adverse events, manage drug safety in both pre- and post-authorization phases, and understand medical device vigilance.
Finally, you will undertake external internships to apply your knowledge in a real-world setting and complete a master’s thesis, consolidating your expertise in the pharmaceutical and biotech industry.