Το Πανεπιστήμιο Λευκωσίας, το μεγαλύτερο πανεπιστήμιο στην Κύπρο, με περισσότερους από 11,500 φοιτητές από 70 και πλέον χώρες του κόσμου, οι οποίοι συνυπάρχουν σε ένα καινοτόμο και πολυεπίπεδο πλαίσιο μάθησης, αποτελεί τον ιδανικό χώρο για να χτίσετε το μέλλον σας.
Με έδρα τη Λευκωσία, την πρωτεύουσα της χώρας, και παρουσία σε άλλες 18 πόλεις σε όλο τον κόσμο, το UNIC, όπως είναι γνωστό, καθοδηγείται από την επιδίωξη της αριστείας στη διδασκαλία και τη μάθηση, την καινοτομία, την έρευνα, την τεχνολογία, και ένα συνεχώς εξελισσόμενο ακαδημαϊκό περιβάλλον.
The program 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 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 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.Programme ObjectivesThe objectives of the programme are to get a thorough understanding of the many aspects of the regulatory process and be able to apply regulations correctly and effectively. In order to achieve these objectives, topics that will be taught include:The principles of drug discovery and drug developmentEU regulation and legislationEU regulatory proceduresMarketing authorization applicationsPharmaceutical regulatory affairs aspects of Pharmaceutical qualityPharmaceutical regulatory affairs aspects of Non-clinical developmentPharmaceutical regulatory affairs aspects of Clinical developmentPharmaceutical regulatory affairs aspects of Quality managementThe future directions in global pharma
Completed application form.Curriculum Vitae.A Bachelor’s degree (accompanied by a transcript) in a field related to Pharmacy, Chemistry, Medicine, Veterinary, Biology from an accredited institution of higher education.A short statement (approximately one page) of personal goals and professional interests.Evidence of knowledge of the English language (I.E.L.T.S band score ? 6.5 or equivalent).Two recommendation letters (one preferably from a University Professor).Other documents that might support the application (e.g. articles, books, awards).Documentation on previous working experience in the Pharmaceutical Industry (if applicable).The admissions process includes an interview with the candidate.