Join Philip Raeth and Polina Shatrova (Palleos) and Valentyna Starodub (Starodub) for an exclusive session on how to design efficient clinical trials through careful budget planning and regulatory guidance for optimal resource allocation, incorporating both strategic designs and tactical monitoring approaches.
🔍 You will learn how to:
✅ Engage with EMA early: Use ITF, Scientific Advice, and ODD for regulatory alignment and optimized trial design
✅ Design efficient trials: Plan recruitment, endpoints, and budget management for cost-effective execution
✅ Accelerate market access: Leverage PRIME, conditional approval, and Adaptive Pathways to reduce development timelines
✅ Optimize resources: Utilize SME Office for fee reductions and regulatory support
✅ Align clinical & financial goals: Incorporate early regulatory feedback to ensure cost predictability and avoid mid-trial redesigns
📅 Date: April 17
⏳ Time: 9:30 am (CET) | 3:30 PM (Beijing time)
Don’t miss this chance to gain expert knowledge and actionable strategies from industry leaders. Secure your spot today!
#clinicaltrials #croeurope #drugregistration #clinicaltrialbudget #euclinicaltrials
Chinese
✈️免费网络探讨会!
解锁欧洲市场：成功注册和临床节省成本的策略
临床研究阶段是药物研发中成本最高的环节。过去十年间，临床试验成本增长了100%，因此，必须通过周密规划和深入理解预算中每一项的底层逻辑来应对这一挑战。
精心设计的预算方案对合同研究组织（CRO）和制药企业的研究成功至关重要。
时间：4月17日下午3:30
欢迎注册交流 http://webinar.palleos.com
