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Egypt Programs

The Course of Studies entitled “Regulatory Affairs of Pharmaceutical Products & Market Authorization” ) is designed as a postgraduate vocational diploma. It is an interdisciplinary diploma covering areas of pharmaceutical sciences, law and medicine. This selective, practical postgraduate diploma is intended to impart knowledge about the chemical, pharmaceutical, pharmacological, toxicological and clinical content of regulatory documentation and its evaluation. The aim is also to provide information on drug development, quality assurance and quality management, pharmaceutical law and on regulatory strategies.
The diploma takes 300 hours of training time. The diploma modules can be taken in about twelve months in a compact way or might be spread across two years at the utmost. The language used in the diploma is strictly English. Attendants are also required to complete tasks & projects of practical nature in the field of Drug Regulatory Affairs.
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Telephone: +(20) 1287668872
Email: contact@sipsmena.com