When: 14 October 2020 | 12:00 BST (GMT+1)
Regulatory intelligence is a novel concept for many in the medical device industry. In recent years, the changes in the global regulatory environment, medical device technology and availability of data on the internet has created an information explosion.
Through this webinar we are aiming to provide a foundational plan for regulatory intelligence capture, analysis and dissemination in the medical device sector for those who are new to the Regulatory Intelligence concept.
After attending this webinar participants will:
- Understand why regulatory intelligence is important for success
- Understand the difference between regulatory information and regulatory intelligence
- Learn how to create intelligence from information
- Get an overview on methods for organisational dissemination
New regulatory recruits (graduates, apprentices)
Professionals new to regulatory affairs (from QA and R&D)
Regulatory Affairs associates, specialists
Regulatory Affairs managers new to medical devices
Individuals new to regulatory intelligence roles
Director, Global Regulatory Intelligence
Kim A. Young, BSc(Hons) MSc, is Director Global Regulatory Intelligence for Instem plc with over 20 years experience in regulatory operations across the medical device, pharma and consumer goods industries.
She is an active member of the TOPRA Regulatory Intelligence Spin Steering Group, DIA Regulatory Information Management Group and a volunteer committee member for the RAPS Euro Convergence 2021 Committee. Kim is also author of a weekly regulatory intelligence blog.
This course offers 1 CPD hours for successful completion. To learn why CPD is important visit our Lifelong Learning page.
How do I register?
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