Paediatric Drug Development: Strategies for Success - Regulatory Framework, Planning and Conducting Paediatric Clinical Trials
Would you like to plan your paediatric clinical trials strategically and conduct them efficiently in practice? Then attend this online seminar and benefit from comprehensive knowledge transfer and the practical experience of paediatric experts!
- Global regulatory landscape for paediatric clinical trials
- Assessment of paediatric investigation plans in the EU: what do the authorities expect?
- Strategic considerations for paediatric clinical trial design: content-related and organisational aspects
- Conducting paediatric clinical trials: hands-on experience
| Veranstaltungs-Code | FB24-524522-61077308 |
Bildungsziel der Schulung:
Paediatric clinical trials are an essential part of drug development. Those who position themselves strategically and plan and conduct the trials carefully will benefit on the drug development timeline.
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In this seminar, you will learn about the regulatory requirements for paediatric clinical trials and how paediatric investigation plans as well as study concepts are assessed in the EU.
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- What are the key design considerations for paediatric clinical trials in terms of preclinical data, toxicology and formulation?
- How can existing data be optimally used in practice?
- And what opportunities are there to involve paediatric patients and their parents in clinical studies - keyword patient-centred study design?
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Attend this seminar to get informed.
Veranstaltungsort:
Online-Webinar
weitere Orte/Termine
Kursart:
Online-Webinar
Kostenlos Info anfordern
