Join our webinar, "Optimizing Cell Therapy Trials of Today: Strategies and Tactics," to explore expert insights on streamlining trial protocols, navigating regulatory landscapes, and optimizing clinical operations. Attendees will gain practical knowledge to overcome common challenges and accelerate the development of innovative cell therapies.
Through interactive discussions, attendees will gain practical insights and actionable strategies to address the key challenges in cell therapy trials. By sharing best practices and lessons learned from industry experts, this webinar will provide participants with the knowledge and tools needed to optimize their clinical trials and overcome common obstacles.
Join us to discuss:
- Cell therapy trials are complex, involving multiple stakeholders, which makes coordination and management challenging. The rapidly evolving nature of cell therapy research demands innovative approaches.
- Optimizing development programs through nuanced protocol development is essential.
- Operationalizing protocols with experienced professionals is crucial to anticipate and address challenges, ensuring trials run smoothly.
Don't miss this opportunity to enhance your cell therapy trial strategies and stay ahead in the rapidly evolving field. Register now for "Optimizing Cell Therapy Trials of Today: Strategies and Tactics" to secure your spot and take the first step towards accelerating the development of life-changing therapies.
Key Learning Objectives
- Understand the complexity and evolving nature of cell therapy trials, including the challenges of multiple stakeholders and the need for innovative approaches.
- Optimize protocol development to minimize amendments, reduce delays, and ensure cost-effectiveness.
- Develop effective regulatory strategies to navigate complex landscapes and maintain compliance.
- Enhance clinical operations and trial execution through best practices in vendor selection, logistics coordination, and expert guidance.
Meet Our Experts
- Amy Raymond, Executive Director, Therapeutic Strategy Lead
- Matthew Confeld, PhD, PharmD, Assistant Director, Clinical Trial Methodology
- Megan Roberts, Director, Project Management, Rare Disease
- Virgilio Garcia Lerma, Executive Director, Global Regulatory Strategist
- Elizabeth Hendryx, Director. Project Management, Oncology and Rare Disease
About Worldwide Clinical Trials
Worldwide Clinical Trials (Worldwide) is a full-service global contract research organization (CRO) that works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. Worldwide’s capabilities include bioanalytical laboratory services, Phase I-IV clinical trials, and post-approval and real-world evidence studies – all powered by an accessible team of clinicians, scientists, and researchers who bring first-hand expertise and a collaborative, personalized approach to each clinical program. Worldwide is therapeutically focused on neuroscience, oncology, rare disease, and cardiometabolic and inflammatory disease. Its global footprint spans over 60 countries with more than 3,600 team members. For more information, visit www.worldwide.com.
