CRED Successfully Navigating European Regulatory Procedures

CRED Successfully Navigating European Regulatory Procedures
A course designed for individuals involved in developing European regulatory strategies for projects or wishing to gain the knowledge and skills to contribute to regulatory strategies.

 9 -10 July 2024
08:30–18:00 BST / 09:30-19:00 CEST

Also available as a face to face course, please click here for the face to face registration option

Course overview

The course is intended to bring the theory and practice of running and working with the EU procedures to life, illustrated with real life examples and case studies.
The course will also cover:

  • Developing your global filing strategy
  • Decentralised and Mutual Recognition procedures
  • Centralised procedure
  • Key EU regional considerations
  • Competent Authority perspective

Benefits to delegates

  • Meet and learn from experts in the field from both industry and agency 
  • Learn by doing - participate in case studies and interactive sessions
  • Build a network to support the rest of your career
  • Gain a firm understanding of the European Regulatory System for medicinal products, developing strategies and HTA 
  • Get practical application of European procedures – an increased focus on the practicalities
CPD: This course provides 17 CPD hours upon successful completion

To learn more about why Continuing Professional Development is important, visit our Lifelong Learning page.


Download a copy of programme here.


Presenters for this course include:

  • Matthew Sardo, Sardo Trading Limited
  • Bob Clay, Highbury Regulatory Science Limited
  • Kora Doorduyn-van der Stoop, Medicines Evaluation Board (MEB)
  • Stephen Smith, GSK
  • Eesha Vyas, GSK
  • Alex Yates, Bicycle Therapeutics
  • Jayne Hunt, Arriello S.R.O
  • Paul Nitschmann, Intercept Pharmaceuticals

Suitable for

  • Those who wish to progress from the introductory course level 
  • More experienced professionals changing area or moving into European submissions
  • Allied professionals for example: Clinical professionals who want to understand the regulatory procedures better and project managers who want to understand the regulatory procedures better.


Simply log in or create an account and register below.
Type Member Non-member 
Standard    £955+VAT  £1,130+VAT

Discounted places
A limited number of discounted places are available at the rates below.
Please email us at for a discount code before making your booking.

Those working for regulatory agencies, government agencies or academic institutions 
Those working for charities, patient groups or in full-time education
 £477.50+VAT  £565+VAT

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

Terms and conditions

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

Next steps

09/07/2024 - 10/07/2024
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