Module 1: September 5-8, 2011 Module 2: February 6-9, 2012 Module 3: June 25-28, 2012 Module 4: September 3-6, 2012 Module 5: February 4-7, 2013 Module 6: June 24-27, 2013
To present a foundation of integrated knowledge in science-based medical product development and regulation.
To enable application of innovative methods, tools and strategies that best utilise recent scientific advances and technologies to medical product design, development and regulatory review.
To address real world challenges encountered during the development, manufacture, review and commercialisation of a medical product.
To cover the entire medical product lifecycle – from molecule to the marketplace.
To train the leaders and integrators for medical product development.
To understand future directions in global pharmaceutical and health economics and business environments, and implications for product development and evaluation.
To provide university, regulatory and industry professionals with a platform and network for the discussion of central issues concerning drug development and new therapies.
To offer the possibility to obtain a Certificate or the title of a University Professional in Pharmaceutical Medicine and to provide the basis and platform achieve a Master in Drug Development Sciences.
To offer the theoretical education for the Swiss speciality recognition for pharmaceutical physicians and the pharmaceutical professionals diploma (since 1999).
To offer a postgraduate examination in pharmaceutical medicine according to international quality standards.