Unified integration

Directly integrates into  IBM Clinical Development's EDC that compiles patient profiles and creates "digital Dossiers".

30% time savings

Digitize your Endpoint Adjudication process and cut your endpoint adjudication timeline processes by 30%.



Interoperable as a standalone solution that can be integrated into any EDC. Can be optimized to study’s need, phase or local regulatory body.

Cut adjudication timelines by 30%

The IBM® Clinical Development Endpoint Adjudication module gives everyone in the adjudication process – sites, coordinators and adjudicators – online access to what they need and when they need it.

The Baim Institute needed to improve the efficiency of the manual, paper-based endpoint adjudication process and incorporated the digital power of IBM Clinical Development’s endpoint adjudication solution. The Baim Institute was able to cut their adjudication timeline by an average of 30 percent and strengthened their relationships with sponsors.

Read the case study

Designed to integrate into your trial

Empower your team and let IBM Clinical Development Endpoint Adjudication compile a digital dossier of all required endpoint details and source documents that can be shared via the cloud instantly.

Designed for interoperability, IBM Clinical Development Endpoint Adjudication is designed to work with IBM Clinical Development's unified EDC platform, or any other EDC that is running your trial.

One Dashboard, Multiple Benefits

IBM Clinical Development Endpoint Adjudication starts with a collaborative workspace that combines various workflows and endpoint management into a single interconnected system. One dashboard lets you manage virtually every aspect of the adjudication process from start to finish.

Get a demo

Manage multi-phase adjudication with ease

  • Experience flexibility and control with customizable endpoint management workflow.

  • Expedite cycle times with online redaction tool and direct, electronic collection of source documents.
  • Improve data quality through eCRFs.
  • Increase convenience for adjudicators with access to assignments and dossiers from anywhere, at any time.
  • Know immediately when documents are ready for review through auto alerts/notifications.
  • Monitor real-time metrics and study listings.

"So why is IBM at OCT Southeast?": We are SO glad you asked!

Of all the questions we heard as a sponsor of last week’s Outsourcing in Clinical Trials Southeast conference, that was definitely the most frequent.

And it’s perfectly understandable. Because while IBM has worked in healthcare for more than half a century (we developed the first pediatric medical record in the 1960s), most of that work has been “behind the scenes” supporting the use of technology in tens of thousands of hospitals, health systems and research organizations worldwide.

Read More

Join IBM to learn best practices in conducting patient-centric trials

Thought leaders from industry and patient-advocacy groups to share methods to optimize trials through stronger patient relationships at national conference.

Patient Centricity, the drive to better align the needs and expectations of both patient and researcher in a clinical trial, is among today’s most important industry issues. Advanced technologies such as smartphones, wearable devices and embedded sensors can help researchers enhance the quality of patient relationships and the timeliness and accuracy of patient-reported data.

Read More