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.
Requirements for Running Clinical Trials in Pediatrics for the EU 2019 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 2019 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