Experienced Adjudicators Across the Globe
Drive effective, unbiased data collection with in‑depth medical oversight and optimized study execution from our expert endpoint adjudication services team.
- In‑depth medical insight and operational precision
- Selection and management of seasoned adjudicator panels
- Unparalleled expertise in renal and cardiometabolic endpoints
- Robust quality control processes across all adjudication projects
- Commitment to industry best practices and continuous improvement
Smart Systems for Smarter Adjudication
Stay on track with efficient endpoint adjudication services featuring technology‑driven workflows and secure systems to support timely and transparent results.
- Centralized endpoint management through the IBM® Clinical Development platform
- CFR 21 Part 11 compliant system available in 50+ languages
- Integrated system for seamless collaboration and visibility
- Option to tailor access by role, site, protocol, and other factors
- Real‑time workflow monitoring and change‑tracking
Flexible & Scalable Clinical Endpoint Adjudication
Achieve consistent excellence from study development through close with flexible, expert‑driven adjudication solutions designed to fit your trial’s unique needs.
- Tailored strategies and workflows to suit every sponsor and trial
- Deep understanding of distinct regulatory landscapes
- Integration with ongoing data management activities
- Project monitoring for consistent quality and efficient delivery
- Endpoint collection, tracking, processing, and reporting
Your Proven Partner from Strategy to Success
We’re with you at every step, from selecting and managing the Endpoint Adjudication Committee to developing endpoint definitions, tailored workflows, and custom web‑based adjudication systems.
Our team also handles endpoint tracking, processing, reporting, and stakeholder training for smooth collaboration.
Case Study
Global Impact with Endpoint Adjudication Services
In the multi‑trial ASCEND program investigating daprodustat for CKD anemia, we partnered with the Duke Clinical Research Institute to manage endpoint adjudication.
By combining our scientific and operational expertise, we addressed fundamental endpoints, supported accurate data collection, and delivered timely adjudication outcomes across:
- 41+ countries
- 8,000+ patients
- 4+ years
Our team’s dedication and experience allowed us to navigate cultural, regulatory, and logistical challenges, contributing to the program’s success— daprodustat met its primary efficacy endpoint in each study.
See our impact in actionFrequently asked questions
What specific services do you offer as part of clinical endpoint adjudication?
We provide tailored services to support your clinical trials, including selecting, appointing, and managing the Endpoint Adjudication Committee and Chair; developing endpoint definitions, adjudication charters, voting forms, and associated documents; customizing web‑based adjudication systems to your trial’s and sponsor’s unique requirements; stakeholder training; and endpoint collection, tracking, processing, and reporting.
How do you maintain transparency in the adjudication process?
Transparency starts with trust, and trust comes from people who care. Our team works closely with you, sharing process metrics and outcomes directly with sponsors for informed decision‑making. You decide which stakeholders can access our endpoint management system, which offers real‑time insights and drives collaboration.
Can access to the endpoint management system be restricted?
Yes, access to the IBM Clinical Development endpoint management system can be restricted. Administrators can limit access based on roles, sites, protocols, or specific permissions, ensuring data integrity and maintaining compliance and security.
Can endpoint adjudication services be integrated with ongoing data management activities?
Yes, endpoint adjudication services can be integrated with ongoing data management activities. Linking adjudication platforms with electronic data capture (EDC) systems and trial databases allows seamless data flow and reduces duplication, streamlining workflows and supporting real‑time insights.
Related Services
Clinical Trial Monitoring
Ensure trial success with expert monitoring and site management, safeguarding data integrity and patient safety through local expertise and oversight.
Regulatory Consulting
Navigate the regulatory landscape with our global team, delivering tailored strategies and efficient clinical trial management from start‑up to safety reporting.
Study Design & Start‑Up
Partner with us to create custom, cost‑effective trial strategies that meet regulatory and sponsor requirements, regardless of project complexity.
Project Management
Drive clinical research success with our experienced project management team, seamlessly coordinating functional areas and vendors across the trial lifecycle.