Industry Insights
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Clinical Trial Design Strategies To Improve Patient Retention
5/27/2025
While clinical trial planning often emphasizes rapid enrollment, sustained patient retention is equally vital to success.
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Critical Imaging Risks In GLP-1 And Neurology Studies
5/27/2025
As imaging grows in importance within GLP-1 and neurology trials, it must be treated not as a routine task but as a strategic pillar that safeguards participant safety and supports robust, reproducible outcomes.
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Inside The Trials Aiming To Stop Vision Loss For Rare Eye Disease Patients
5/27/2025
Ocugen Chief Medical Officer Huma Qamar, MD, MPH, CMI, discusses two rare disease trials and how the company's managed their protocol design, PI selection, and patient recruitment.
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The Makings Of 'Regulatory-Grade' RWD In Ophthalmology Using AI
5/25/2025
Regulatory bodies like the FDA and EMA now prioritize real-world data in clinical research. Learn more about its value in enhancing drug development, regulatory decisions, and patient outcomes.
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How AI Is Helping Transform Neurodegenerative Disease Treatment
5/23/2025
In today’s healthcare landscape, the focus of real-world evidence has shifted from sheer database size to the quality, granularity, and actionable insights derived from detailed, de-identified patient-level data.
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Bayesian Study Designs In Early-Phase Oncology Trials
5/23/2025
In response to insufficient traditional dose-escalation methods, regulatory initiatives like the FDA’s Project Optimus advocate for identifying optimal biological doses rather than relying solely on maximum tolerated doses (MTD).
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Reimagining The Protocol For The Future Of Research
5/23/2025
Clinical trial protocols are the blueprints of research, yet they remain locked in static, text-based documents that must be manually reinterpreted across each clinical system.
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No Patient Left Behind: Personalized Travel Support
5/23/2025
In the dynamic realm of clinical research, patient-centricity is paramount. Concierge services help to support patients by coordinating travel, handling reimbursements, and meeting complex needs.
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Don't Miss These 2025–2026 EMA IDMP Compliance Deadlines For Product Management Services
5/22/2025
The EMA's Product Management Services will serve as a comprehensive database for consistent identification of medicines internationally. One deadline is quickly approaching on May 31. Are you ready?
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Clinical Trial Payments And Ethics: Your Top Questions Answered
5/22/2025
In response to widespread uncertainty around ethical clinical trial payments, this article explores foundational questions surrounding participant compensation.