From The Industry Experts
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Solving Trial Enrollment Challenges With Direct-To-Patient Recruitment
1/6/2026
Overcome enrollment bottlenecks by shifting from site-centric models to tech-enabled, direct-to-patient outreach.
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How Rescue Studies Use Direct-To-Patient Strategies To Accelerate Clinical Trial Enrollment
1/6/2026
If your trial struggles to overcome enrollment bottlenecks, a tech-enabled rescue strategy could be the solution.
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Why We Need To Look To The Future Of Clinical Trials
1/6/2026
Explore how decentralized trial elements, community-focused site networks, and patient-centric infrastructure can improve recruitment, data quality, equity, and efficiency.
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How DCTs Can Shift The Pediatric Rare Disease Research Landscape
1/6/2026
DCT solutions are not just about bringing the trial to the patient’s home and reducing logistical burdens, but also strengthening the family-researcher connection.
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Reducing The Burden Of Patient Retention And Improving Continuity
1/6/2026
Immunology trials often place a sustained burden on participants. However, integrating Home Trial Support (HTS) into a Phase 3 immunology trial can help improve the overall study experience.
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A New, AI-Augmented Horizon For Safety And Pharmacovigilance
1/6/2026
Is your organization leveraging AI to maximize efficiency in safety and regulatory workflows? If not, explore how these technologies are slated to improve industry approaches in 2026.
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Psychiatric Drug Development Renaissance: With Familiar Risks
1/6/2026
Emerging psychiatric therapies bring hope, but progress is fragile. Biomarker-driven, mechanism-first approaches help overcome biological, regulatory, and commercial barriers.
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Trailblazing Clinical Drug Development In Dermatology
1/6/2026
AI, imaging, and biomarkers are transforming trials, reducing subjectivity and improving sensitivity while enabling decentralized designs, faster timelines, and more precise insights.
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Clinical Research Trends And IRB Expectations For 2026
1/6/2026
Oversight in 2026 requires adaptability as AI, consent standards, and regulatory uncertainty challenge sponsors and IRBs to balance ethics with innovation through proactive planning and collaboration.
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Medical Insight's Role In Early-Phase Clinical Development
1/6/2026
Medical insight reduces risk, strengthens protocols, and accelerates timelines — enhancing safety, feasibility, and collaboration for successful trials and reliable outcomes.