Requirements for Running Clinical Trials in Pediatrics for the EU

Laura Brown

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Why Should You Attend:

This webinar will provide critical assistance to FDA and EMA regulated companies currently carrying out or preparing to conduct clinical trials in pediatrics in the EU. 
This presentation cover recommendations on various ethical aspects of the performance clinical trials for treating, preventing or diagnosing a disease or condition in pediatrics. 
The speaker will explain how to ensure pediatric studies must be child and family-focused if they are to run safely, smoothly and to schedule by complying with the EU Clinical Trial Directive guideline which provides excellent guidance on how to run ethically sound clinical trials in children. A practical, step-by-step guide to running successful clinical trials in pediatrics will be provided to help ensure compliance.


Areas Covered in the Webinar:

  • Learn how to plan and manage successful clinical trials in paedeiatrics
  • Understand the latest regulatory guidelines and how it will impact your clinical trials in practice
  • What are the considerations for consent and assent?
  • What are the practical requirements for running paediatric clinical trials?
  • Appreciate the demands of paediatric populations and how this will impact your trial
  • What are the special requirements for ethical review?
  • How to reduce fear and distress?
  • What are the recommendations for bodyweight and volumes of blood that can be taken?
  • How to avoid unnecessary duplication of trials?
  • What about the standards for non-EU countries for running clinical trials?


Who Will Benefit:

This webinar will provide critical assistance to FDA and EMA regulated companies currently carrying out or preparing to conduct clinical trials for pharmaceutical, biotechnology, and biologics products in paediatrics.

  • Clinical Development managers and personnel
  • Clinical research associates
  • Clinical Research archiving and document management personnel
  • Quality assurance managers and auditors
  • Clinical Development managers and personnel
  • Consultants
  • Regulatory Affairs professionals
  • Academic clinical trial sites

Webinar Events
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Training CD-DVD

Physical CD-DVD of recorded session will be despatched after 72 hrs on completion of payment

Recorded video

Recorded video session

Speaker: Laura Brown, Independent QA and Training Consultant, Laura Brown Tra

Dr Laura Brown is an independent Pharmaceutical QA, Management and Training Consultant, and Course Director for the MSc in Clinical Research, School of Pharmacy at the University of Cardiff. Laura has more than 20 years' experience of Quality Assurance and managing international clinical trials including risk identification and management and risk based monitoring. She has worked for several companies including GSK, Hoechst Marion Roussel, Good Clinical Research Practices and Phoenix International. She has consulted with numerous pharmaceutical companies, suppliers to the pharmaceutical industry as well as academic institutions.

Dr Brown has an MBA with specialization in project management including risk management. She is also the external project management expert for a pharmaceutical e-learning MSc module in project management covering risk management, and the author of two books on project management including the leading book “Pharmaceutical Project Management” (Gower).

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