Overview of EU Pharmaceutical Regulatory Affairs

Overview of EU Pharmaceutical Regulatory Affairs
Module 0 of the MSc:  This course covers all aspects of the product development process, and provides a sound overview of EU legislation and regulatory procedures, including the central role regulatory affairs plays in modern healthcare companies.

When:
16-19 April 2024
Where: ETC Venues, London



Please note that the course will include pre-work.

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

  • Four interactive days with comprehensive range of topics and case studies
  • Develop a network to support the rest of your career
  • Meet and learn from an international speaker panel from agencies, industry and contract houses 
  • High quality course materials 
  • Gain the practical skills to be a highly effective regulatory professional 
  • Industry-wide recognised programme will be an excellent start to your career
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.  

Programme

 You can view and download the course programme here.

Module Leaders

                                                                             

Sacha  Lynch, Principal Consultant, DLRC

Grzegorz Kojro, CDM Manager, Pfizer

 

Presenters


     Dima Al-hadithi

     Mirza Catibušic
 
     Shaila Choi
 
     Brian Corrigan

      Jennifer Davies

     David Jones 

     Chris Powell

     Richard Keane

     Niamh Lawler-Turner

     Kay Martin

      Steve Pinder

    
 


 

Suitable for

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

Pricing

Standard

  • Member: £2,775 + VAT* 
  • Non-member: £3,165 + VAT*

Save the full cost of membership and £180 when you add TOPRA membership to your booking. Please note: membership fees are exempt from 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.

Discount prices:

  • Those working for regulatory agencies, government agencies or academic institutions:
    • Members: £2,081.25 + VAT*
    • Non-members: £2,373.75 + VAT*
  • Those working for charities, patient groups or in full-time education:
    • Members: £1,387.50 + VAT*
    • Non-members: £1,582.50 + VAT*

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

Terms and conditions

By booking a place on this course you are agreeing to the training terms and conditions

 

When
16/04/2024 - 19/04/2024
Where
ETC Venues 86 Edgware Road London W2 2EA UNITED KINGDOM
Sign in or create an account to register Last day to register is 12/04/2024
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Important instructions before booking - If your company name or VAT number does not appear here or you would like to be invoiced using a different VAT number, please email finance@topra.org

Tuesday, 16 April 2024

Description
16/04/2024

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