Requirements for Running Clinical Trials in Pediatrics for the EU

Requirements for Running Clinical Trials in Pediatrics for the EU is a webinar dedicated to compliance requirements for running clinical trials in pediatrics, particularly in the EU.

Requirements for Running Clinical Trials in Pediatrics for the EU covers topics such as:

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

Requirements for Running Clinical Trials in Pediatrics for the EU is intended for:

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

Future Events

Requirements for Running Clinical Trials in Pediatrics for the EU 2020

Important

Please, check the official conference website for possible changes, before you make any traveling arrangements

Prices are for evaluation only.

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