CRED Understanding Clinical Development

CRED Understanding Clinical Development
This two-day workshop will provide an overview with practical advice from regulators and industry on the process of designing and conducting clinical trials from phase I through phases II, III and even clinical trials considerations beyond drug marketing approval.

:  15-16 October 2024
Where:  TOPRA Office, 3 Harbour Exchange, London, E14 9GE, United Kingdom
Time:  09:20 GMT/ 10:20 CET 

Course overview

The aim of this practical workshop is to enable all those involved in medicines development to gain an appreciation of the points to consider when designing a clinical development programme to support a marketing application and also that clinical development extends beyond the marketing application.
This course will cover:

  • Clinical pharmacokinetics
  • Clinical Pharmacodynamics
  • Optimal study design
  • Paediatric Investigation Plans
  • Safety

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
  • An opportunity to ask questions and have an open discussion with speaker and delegates
  • Optimise your clinical development programme 
  • Design clinical trials to support proof of efficacy 

CPD: This course provides 15.50 CPD hours upon successful completion

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


Download a copy of the course previous programme here.


Past Presenters include:
  • Beatrix Friedeberg, Janssen Pharmaceuticals
  • Glyn Belcher, PV Consultancy Ltd
  • Steve Pinder, Envestia Ltd
  • Tomáš Radimerský, State Institute for Drug Control (SUKL)
  • Marco Siccardi, Labcorp
  • Carly Barraclough, Amgen Ltd

Suitable for

  • Less experienced regulatory professional who requires comprehensive information on this subject
  • Experienced professional who is a newcomer to this subject
  • Those who wish to update their knowledge on this subject
  • Persons from regulatory, medical, clinical and safety functions involved in phase I, II, III and IV trials.


Simply log in or create an account and register below.
Type Member Non-member 
Standard    £955+VAT  £1,130+VAT
Add membership to your booking to access the members' discount. 

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


15/10/2024 09:20 - 16/10/2024 16:30
TOPRA 6th Floor 3 Harbour Exchange London E14 9GE UNITED KINGDOM
Sign in or create an account to register Registration ends 14/10/2024 09:00 (GMT Daylight Time)
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Tuesday, 10 October 2023


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