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: 15-17 April 2025
Where:
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 draft course programme here.

Module Leaders


     

Sacha  Lynch, Principal Consultant, DLRC

 
 

     

Grzegorz Kojro, CDM Manager, Pfizer

 

Presenters


     Dima Al-hadithi
     Mirza Catibušic
 
     Shaila Choi		     David Jones 
     

      Jennifer Davies
         Steve Pinder  

     Chris Powell
     Richard Keane

     Niamh Lawler-Turner
     Kay Martin



    
 


  

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: £2,200 + VAT* 
  • Non-member: £2,600 + VAT*
  • TOPRA MSc Student: £2,000 + 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: £1,650 + VAT*
    • Non-members: £1,950 + VAT*
  • Those working for charities, patient groups or in full-time education:
    • Members: £1,100+ VAT*
    • Non-members: £1,300 + 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
15/04/2025 - 17/04/2025
Where
UNITED KINGDOM
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