After completing this 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
EUPATI Open Classroom content is free for all learners. At the end of each course you can test your knowledge and earn a certificate for a 10-euro administrative fee. If interested, click the button below: