Essentials of EU Regulatory Intelligence
- Mission, organisation and value of the Regulatory Intelligence function in a pharmaceutical company
- Overview of the various sources/types of information and different ways to collect it (Push vs. Pull models)
- Collaboration between corporate RI function and local stakeholders
- Assessment of the relevance
- Time-sensitivity and impact of information on the company’s processes and business
- Interactive session on practical case studies (point of view of several RI professionals on key topics)
- Analysis of the strengths and weaknesses of the different media available for dissemination of the information (Newsletters, Intranets, Social media…)
- Discussion on how to store curated information and how to integrate Hard Intelligence and in-house Soft Intelligence
- Regulatory data analytics: Can technology take it one step forward?
Who should attend?
Professionals that are interested in developing regulatory intelligence skills and possibly specializing in that field are provided with a comprehensive and focused teaching experience. The goal is to master regulatory intelligence as described in DIA’s definition of the term as “the act of gathering and analyzing publicly available regulatory information (…) including communicating the implications of the information, and monitoring the current regulatory environment for opportunities to shape future regulations, guidance, policy, and legislation.”
Get an overview of key aspects of regulatory intelligence with hands-on knowledge.
Learn how to gather the right information and understand the impact on your organization.
This training course provides you hands-on experience in:
- identifying the most reliable and valuable sources of information
- monitoring selected sources
- assessing the impact of new requirements on your business
- communicating key intelligence to internal stakeholders
- saving time and resources with the right sources and strategies
- understanding the strategic value of regulatory intelligence