Pharmaceutical science is an interdisciplinary field that focuses on the interactions of drugs with the human body. Students in this field may learn how to modulate interactions so as to provide better and safer drug products and therapies targeted at human disease.
Across the Atlantic, the discussion about online courses and their potential to restructure higher education has been raging for some time. Courses are structured as weekly online conferences; communication with the course tutor and other learners takes place in a virtual learning environment. The online courses are intended to fit around your calendar; you access the course whenever it is suitable for you.
The programme is an international master’s program on the regulation of medicinal products, biological and biotechnological products as well as on the regulation of other
Duration: 1.5 Years (3 Semesters)
Qualification Awarded: Master of Science in Drug Regulatory Affairs
Level of Qualification: Master Degree (2nd Cycle)
Language of Instruction: English
Mode of Study: Distance Learning
Minimum ECTS Credits: 90
The programme is an international master’s program on the regulation of medicinal products, biological and biotechnological products as well as on the regulation of other health care products i.e medical devices and herbal medicinal products.
The program targets individuals involved in the regulatory and legislative areas of the pharmaceutical industry, as well as employees in healthcare and biotech companies or in regulatory bodies. Candidates will gain a comprehensive and detailed knowledge of the procedures related to the application, registration, and approval of drugs and biological and biotechnological products that will qualify them to specialize in the entire process of drug registration from the initial stages of discovery to final approval and to the post-marketing surveillance. Programme participants will thus be qualified to advise and involve professional groups in the development process surrounding the regulatory and statutory requirements governing drug registration, potentially shortening the length of time it takes for companies to obtain a marketing approval and managing the drug on the international market. Also, the programme offers the opportunity for continuing professional development of persons already employed in this field at the junior level....