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Expert panel: Smarter clinical labeling for faster clinical trial startup
Watch this webinar to discover how clinical trial teams can optimize label development, translation, and production to help streamline study startup and achieve first-patient-in (FPI) milestones faster.
Clinical trial teams face growing pressure to reduce startup timelines while maintaining quality, compliance, and operational efficiency as programs progress. Yet label development, translation, and production remain critical-path activities that can delay first patient in (FPI) and impact key study milestones.
This on-demand webinar—originally hosted by Citeline—features an expert-led panel discussion exploring today’s clinical labeling challenges and practical strategies to help streamline trial startup.
Through a moderated conversation, Thermo Fisher Scientific’s industry specialists share best practices, discuss evolving industry trends, and examine how optimized labeling workflows can help reduce complexity and improve execution across global studies. Watch the webinar at your convenience to learn more.
What you’ll learn in this webinar on smarter clinical labeling for faster clinical trial startup:
- How to identify and address labeling challenges that can delay startup and FPI
- Proven strategies to help optimize the clinical label design and ordering process
- Ways to utilize smarter workflows to help accelerate clinical trial startup timelines
- The benefits of both global and in-region manufacturing of clinical trial labels
Panelists:
- Julia Field, Senior Product Manager, Global Label Services, Thermo Fisher Scientific
- Dana Chatrie, Label Program Manager, Thermo Fisher Scientific
- Mike Donahue, Senior Label Program Manager, Thermo Fisher Scientific