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: TOPRA Office, 3rd Floor City Reach, Greenwich View Place, London, E14 9NN, UK
TIme: TBC

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 three-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


  
   
   
   
 



    
 


  

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

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 for those:

  • in low income countries as defined by the World Bank
  • working for regulatory or government agencies, charities, academic insitutions or NGOs. 
  •  

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

 

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
TOPRA 3rd Floor City Reach 5-6 Greenwich View Place London E14 9NN UNITED KINGDOM
Sign in or create an account to register Last day to register is 14/04/2025
My registration status: Not registered
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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

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