When: 12-15 November 2024
Where: Ramada, Avenida Engenheiro, Arantes e Oliveria 9, Lisbon, Portugal
This course is essential for:
- People new to Regulatory Affairs who want to acquire a comprehensive foundation
- Regulatory professionals wishing to update their knowledge
- Allied professionals wanting to understand the role of Regulatory Affairs
Course information
TOPRA's Introductory Courses have been designed to provide a firm foundation to your career in regulatory affairs. They are the most comprehensive of their kind and are presented by speakers and facilitators from industry and agencies, all respected authorities in their field. Our four-day Overview of EU Pharmaceutical Regulatory Affairs course (formerly known as the The Spring Introductory Course) covers all aspects of the product development process and provides a sound overview of EU legislation and regulatory procedures, plus explores the central role regulatory affairs plays in modern healthcare companies and the development cycle of new drugs.
Note: This course is also Module 0 of the MSc Regulatory Affairs.
Benefits for delegates
CPD: This course provides 30 CPD hours upon successful completion. To learn more about why Continuing Professional Development is important, visit our Lifelong Learning page.
Terms and conditions
By booking a place on this course you are agreeing to the training terms and conditions.