Requirements for Running Clinical Trials in Pediatrics for the EU 2019

Requirements for Running Clinical Trials in Pediatrics for the EU 2019 is a webinar dedicated to compliance requirements for running clinical trials in pediatrics, particularly in the EU.

Topics

• 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?

Who should Attend

• 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