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.