Insights On Trial Design
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Redefining Accessibility For Pediatric Patients
9/24/2025
Explore how meeting patients where they are can redefine what successful pediatric trial delivery looks like.
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Linking Neurology And Ophthalmology For Clinical Trials
1/22/2025
Learn more about the innovative approach being taken to incorporate ophthalmology into neurology and central nervous system (CNS) research.
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Solutions That Successfully Drive Results: Stories Of Delivering Clinical Trials Wherever Patients Live
10/28/2025
This session focuses on how to implement solutions that deliver trials without boundaries aimed at reducing participation burden for sites and patients.
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Professional Services Expedite Hospital's Study Process
11/17/2023
Explore the details of a transformative partnership where a children's hospital was able to overcome coverage analysis and budget negotiation issues despite a significant staff turnover.
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Streamlining Phase 1 Trials With The Mobile Vision Pod
1/29/2025
A contract research organization formed a partnership to address significant challenges during a Phase 1 clinical trial for a corneal disease treatment through the use of a Mobile Vision Pod.
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Could Adoption Of Mobile Nurse Visits Lead To Faster Study Results?
11/21/2023
As sponsors seek to minimize trial delays and get new therapies to market faster, explore whether increased adoption of a more patient-centric approach could make a difference to timelines.
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The Next Frontier In Early Phase Oncology Trials
10/18/2024
This session explores the pivotal role of First-in-Human and early phase oncology trials in drug development, emphasizing the importance of comprehensive planning for successful execution.
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Diversity At The Start: Best Practices For Clinical Trial Planning
9/9/2024
Claire Riches, Citeline's VP of Clinical Solutions, emphasizes that clinical trial diversity must start with a fit-for-purpose protocol, incorporating the patient voice early on to ensure success in reaching diverse populations.
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Three Ways To Accelerate From Trial To Market
1/9/2025
Moving from pre-IND to IND involves preparing for FDA interactions with a focused pre-IND meeting request and package, Selecting the right CRO, and ensuring data integrity.
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From Crisis To Confidence: Ensuring Smooth Regulatory Submissions
10/8/2024
Explore some of the major challenges that medical writing submission specialists face today and strategies that can consistently set the stage for success.