Global Clinical Trial Management
Clinical trials are an enormous undertaking. They can involve thousands of people, hundreds of investigative sites, multiple CROs, and various eClinical source systems ─ all generating massive amounts of data.
See how OnPoint CTMS transforms a disjointed clinical trial into an efficient and cohesive work environment with Microsoft – the most pervasive office productivity tool in the world.
OnPoint CTMS is a powerful end-to-end clinical trials management solution that brings control, efficiency, and quality data to every study. This web-based CTMS works on the go, letting you view and manage real-time operational performance — wherever and whenever.
Leverage Microsoft Assets
OnPoint is Microsoft Office-smart. It lets you leverage your everyday Microsoft Office tools to access, update, and report on study data, as well as track and manage study activities securely and compliantly — only part of the reason OnPoint is the CTMS of choice for life sciences companies around the globe.
OnPoint makes it easy to connect to clinical trial data through Outlook, export to Excel and collaborate in a secure way using direct connection to SharePoint. Document updates done in SharePoint are automatically reflected in OnPoint so that your trial data is accurate, current, and in synch. And since most OnPoint interaction is through familiar Microsoft applications, users work in a way they’re accustomed to and training is minimal.
Better Workflow, Deep Savings
OnPoint vastly improves efficiencies in both data flow and work flow, yielding cost-savings in time, labor, and operational expenses. Moreover, integrating Office processes with clinical operations can reduce back-office paperwork and significantly lower administrative overhead. And leveraging existing Microsoft investments means total cost of ownership is low.
End-to-End Clinical Trial Management
OnPoint CTMS connects the many moving parts of the clinical trial process and lets you monitor progress from a central dashboard. OnPoint manages the clinical trial right from the start and maintains role-based access controls across the continuum, from study design, through close-out and FDA submission. This end-to-end clinical trial management solution includes the tools to plan, startup, conduct, and manage your study, and complete monitoring and regulatory compliance activities. It supports every study aspect, whether design, procedures, protocol, study arms, visits, forms, treatments, payment, and more.
Get an in depth look at OnPoint’s robust features and functions.