Earn an MSc in Drug Regulatory Affairs Online

at the First University in Europe with 5 QS Stars in Online Education

Request Information

MSc in Drug Regulatory Affairs

Duration
3 Semesters

Qualification Awarded
Master of Science in Drug Regulatory Affairs

Language
English

Mode of Study
Distance Learning

  • Skilled Regulatory Affairs professionals are in high demand
  • The first MSc in Drug Regulatory Affairs in Southern Europe and the Middle East

  • Ideal for both working professionals and new graduates

  • Fully online Master’s Degree from the first University in the EU to receive a 5-star rating for Online/Distance Learning

  • Focused on global outreach through engagement with regulations in the EU, US and emerging markets

  • Flexible learning tailored to your needs and designed to meet the current demands of the pharmaceutical industry

The Drug Regulatory Affairs (MSc) is an international master’s programme focusing on the regulation of medicinal, biological and biotechnological products, as well as on the regulation of other health care products i.e. medical devices and herbal medicinal products.

The programme targets individuals involved in the regulatory and legislative areas of the pharmaceutical industry, as well as employees in healthcare and biotech companies or in the regulatory bodies.

Graduates of the programme will be qualified to advise and involve professional groups in the development process dealing with the regulatory and statutory requirements governing drug registration.

Featured Faculty

“Regulatory affairs are integral to the registration and approval of pharmaceutical products in an increasingly demanding legislative and competitive environment. The Drug Regulatory Affairs programme from the University of Nicosia will provide the participants with a comprehensive overview of the complex regulatory landscape across all phases of the drug development process. The programme graduates will be able to contribute to the registration of safe and effective medicinal products in compliance with stringent regulatory requirements”.

Anastasia Sideri, PhD, Medical Advisor, Medical Affairs, Zeincro Hellas SA

“Regulatory Affairs (RA) professionals play a critical role in the pharmaceutical industry since they are the ones responsible for a healthcare product’s lifecycle, providing strategic and operational direction and support to work within the regulations and guidelines to expedite the development and delivery of safe and effective products worldwide. The demand for RA professionals is evident across the pharma industry, consultancy companies, regulatory agencies, and clinical research organisations. The postgraduate course at the University of Nicosia offers high-quality education for people who would like to follow this career pathway. In addition, the programme is structured in such a way that it offers those already employed in this field at a junior level the opportunity for continuing professional development”.

Christiana Kitromilidou, Regulatory & Pharmacovigilance Manager

The University of Nicosia in Numbers

0
QS Stars for Online/Distance Education
0+
On-Campus and Online Students from Over 70 Countries
#0
Ranked University in the EECA Region
#0
Largest University in Southern Europe that teaches primarily in English
#0
in the World for Blockchain & Digital Currency
0
Research Centres
0+
Student Mobility University Partners
0+
Bachelor, Master and Doctoral Degrees

UNIC is a Distance Education Leader With the Highest Accolades