Programme content

The programme provides the regulatory and economic framework and the most important processes from the pharmaceutical/biotech/medical device development to the marketing of a drug product. Experienced speakers from industry, consulting and the health authorities ensure that the course contents are practice-oriented and are covered from different points of view. This provides a comprehensive understanding of the complex contexts and state-of-the-art contents.

The modules consist of lectures, workshops, case studies and plant visits.

The topic areas of the programme include:

  • Pharmaceutical/biotech/medical device development and production
  • Quality management and GxP (Good Manufacturing Practice etc.)
  • Preclinical and clinical development
  • Regulatory affairs
  • Project management
  • Healthcare Systems, Pharma/Biotech/Medical Device Business and Marketing
  • Communication

For the detailed learning objectives please see under the respective module.

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