After completing the course, you will be able to:
-
Describe the components of product information and access to information they contain
- Outline the legal mandate and review process of product information
- Explain the difference between advertising and promotion of medicines to the general public and healthcare professionals with reference to the legal framework
-
Explain the relation between different levels of Codes of Conduct and their differentiation to Codes of Ethics
- Relate the EFPIA Code of Practice to the underlying EU Directive 2001/83
Duration: 8 hours
