Trial Design Solutions
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Castor Professional Services: Your Trial Delivery Partner
3/17/2026
Accelerate clinical trial timelines and ensure audit-readiness with expert-led build models, AI-driven data management, and global participant support designed to streamline your path to submission.
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Supporting Patients For Better Clinical Trials
5/6/2025
From our inception, Ergomed has been committed to enhancing the patient journey in clinical trials. Our unique Ergomed CARE™ approach revolutionizes trials by optimizing the patient experience. Designed to address and resolve issues proactively, this comprehensive approach supports and engages all stakeholders, leading to accelerated study start-up, improved patient recruitment and retention, and investigator engagement.
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Develop Site-Centric Protocols To Optimize Enrollment And Maximize Performance
4/10/2026
Optimize clinical trial protocols by aligning scientific goals with real-world site operations. Improve patient enrollment, reduce site burden, and minimize costly amendments through data-driven design.
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Accelerating Patient Recruitment In Oncology Since 2005
12/17/2024
CSSi is a global, full-service company offering customized services to support recruitment and retention programs around the world.
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Navigating The Use Of Controlled Substances In Clinical Trials Using IRT
Sponsor organizations that want to use controlled substances in clinical studies must manage the associated regulatory and logistical requirements. Read how this can be challenging for emerging biopharma.
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Why Central IRBs Matter For Efficient Clinical Trials
4/10/2025
“Going the extra mile is a big part of our DNA. Personal attention can go a long way in ensuring the success of your next research study.”
Raffaella Hart, MS, CIP
Sr. Vice President, IRB and IBC ServicesFast, reliable IRB review for multisite studies backed by expert oversight and responsive support. With streamlined submissions, frequent meetings, and dedicated client managers, BRANY IRB helps you save time and money while maintaining full regulatory compliance.
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Early Phase Clinical Trials
10/21/2025
As a full-service contract research organization, Southern Star Research has the knowledge, industry relationships and technical expertise to get your early-phase clinical trial up and running safely and efficiently.
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Post-Marketing Studies And Real-World Evidence Clinical Trials
4/9/2026
Your trusted partner for decentralized post-marketing surveillance clinical trials and real-world evidence collection. Point-of-need accessibility. Proven compliance.
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Accelerate Clinical Trial Cycle Times With Citeline Study Feasibility
6/29/2021
Citeline Study Feasibility is a platform that combines subject-matter expertise and machine learning to develop predictive insights for feasibility planning. Clinical trial sponsors can use these insights to identify key data drivers and model their impact, build and simulate feasibility scenarios, accelerate timelines, and make better decisions than with statistical methods alone.
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Accelerate Approval Of Novel Therapies
8/9/2023
Learn how to make critical, data-driven decisions throughout the product development lifecycle and increase new therapies' probability of success.