Webinar: Developing Medical Device Regulatory Intelligence

Webinar: Developing Medical Device Regulatory Intelligence
This webinar is designed to support those new to the Regulatory Intelligence concept in the medical device sector and to provide a foundational plan to anyone looking to take their first steps in assuming primary responsibility for regulatory intelligence in their organisation.


When:
 Available on demand. (Originally presented in October 2020.)

Overview

Webinars photoRegulatory 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.

 

Learning objectives

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
     

Target Audience

  • 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

Speaker

Kim Young
Director, Global Regulatory Intelligence
Instem plc

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.

 

CPD

This course offers 1 CPD hours for successful completion. To learn why CPD is important visit our Lifelong Learning page.

How do I register?

Simply log in or create an account and register below. 

Prices

Type Member  Non-member 
Standard    £70 + VAT £95 + VAT 
 

Discounted Places

A limited number of discounted places are available at the rates below for those:

Please email meetings@topra.org for a discount code before making your booking.

Type Member  Non-member 
Discount  £35 + VAT*  £47.50 + VAT* 


* VAT, if applicable, is charged at a rate of 20%.

Terms and conditions

By purchasing this webinar, you are agreeing to the terms and conditions.

When
14/10/2020
Where
Miscellaneous ONLINE
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