Reserve your spot and experience a facilitated discussion regarding solutions to your regulatory challenges. To reserve your spot you must select it during registration: Visit the website to modify your registration! Due to popular demand, space is limited to 20 people per solutions circle. There is no fee, but reservations are required. Open to paid delegates only.
This session intends to provide an overview of key aspects of regulatory intelligence (RI).
It will focus on identifying the most reliable and valuable sources of information, monitoring selected sources, assessing the impact of new requirements on the company’s business and adapting the way of communicating key intelligence to the needs of internal stakeholders.
The session will concentrate on the EU environment and its key stakeholders, such as the European Medicines Agency (EMA) and the European Commission (EC) and will explore the sources and types of available information that can support regulatory strategies and wider R&D discussions.
Learnings from this session will allow foundational and intermediate regulatory affairs professionals to participate in thoughtful discussion on the fundamentals of regulatory intelligence and to enhance their own careers.
Learning Objectives:
Correctly identify current key aspects related to the monitoring, impact assessment and internal communication of EU regulatory intelligence
Successfully navigate relevant sources of information and refine their regulatory intelligence skills
Better understand the strategic value of regulatory intelligence
