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.

When:  14-15 October 2025
Where:  Online
Time:  9.00 a.m. BST



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

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.

Programme

Download a draft copy of the course programme here.

Presenters

Past Presenters Include:

  • Beatrix Friedberg, Vertex Pharmaceuticals
  • Steve Pinder, Envestia Ltd
  • Marco Siccardi, ESQlabs
  • Carly Barraclough, Amgen LTD
  • Janet Jepras, Janet Jepras Consulting 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.

Pricing  


Simply log in or create an account and register below.
Type Member Non-member 
Standard    £1,050 +VAT  £1,250 +VAT

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

  
Those working for regulatory agencies, government agencies or academic institutions 
  £787.50 +VAT
  £937.50 +VAT
Those working for charities, patient groups or in full-time education
  £525 +VAT  £625 +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
When
14/10/2025 - 15/10/2025
Where
Online
Online registration not available.
Your company name
Your VAT country
Your VAT number
NOTE
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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