- Why SureClinical
Our Eclinical Ecosystem components include our Eclinical Applications, our Eclinical Collaboration Platform and our Eclinical Intelligence Suite.
Automate, streamline and accelerate clinical operations and quality with our suite of connected clinical applications for project management, quality, and regulated content management for sponsors, CROs and investigator sites.
Our Eclinical Collaboration Platform connects teams with applications and productivity tools such as trusted office document signing, trusted web meetings, automated workflows, forms and a private team network.
Automatically connect, capture, combine and monitor clinical performance metrics and analytics in a single flexible clinical knowledge repository.
CTMS Clinical Trial Management System
Automate Clinical Trial Operations
The phrase ‘make a plan and work it’ has never been easier than with SureCTMS, the only clinical trial management system part of a unified Clinical Operations Suite including ETMF, Adobe Certificate Signing, a private trusted clinician network and connectivity to nearly any enterprise application, database or data source. Our template-based project startup wizard gets you started in minutes, not months. Milestone management dashboards manage and control up to thousands of workflows concurrently, letting you automate enrollment, monitoring and reporting. Monitor visit report automation is linked to real-time analytics and notifications. Connect with popular EDC systems for real-time study subject data import. Designed as a mobile-first application, SureCTMS provides clinical trial project managers and global team members with easy to use, always available tools to manage clinical trial projects at the point of activity. Whether you’re at a site, in the office or on the go – SureCTMS helps you to manage projects anytime, anywhere
Optimize your study, site, and team management
In order to accelerate new drug development project timelines and to lower costs, clinical trial projects need to get started faster and finish sooner.
To shorten project timelines, SureCTMS automates common clinical trial management tasks such as essential document collection, site visit scheduling, activities, tasks and monitor reporting; site payment tracking and issue management. SureCTMS is the first CTMS system to address the entire clinical trial management lifecycle with a suite of unified applications and a trusted clinician network. From searching for qualified investigators in our trusted clinician network to the FDA submission process, your team will be able to more efficiently analyze, execute, track and automate common clinical trial tasks.
Accelerate Study Startup
After product efficacy, effective study team selection is cited as the single most significant success factor in clinical trials. With SureCTMS™, SureNetwork™ and our unified platform, you can quickly search, identify, qualify and recruit sites and study team members with the right experience and verified credentials. Identify your dream study team and bring them directly into your CTMS project with the click of a button.
Study Process Automation
Milestone and Activity Automation
Automate recurring activities such as site visits, monitor visit reporting, follow-up letters and more with activity plan templates, task workflow automation and project calendars. Track task execution and progress with real-time Gantt milestone charts, proactive task notifications and reporting.
Unified CTMS and ETMF
Manage and Track Essential Docs
Simplify clinical study document collection, completion and tracking with SureETMF, our premier next generation cloud ETMF solution. Save time with a unified solution offering a single source of truth. Both SureETMF and SureCTMS are FDA compliance validated.
CTMS Study Creation Wizard
Get your new study started in minutes, not months. SureCTMS study creation wizard sets up and configures your CTMS, ETMF, Study Team and more in as little as 5 minutes. Quickly start a study without expensive setup fees, consulting fees or implementation fees. Save study templates for reuse across other projects.
Single Source of Truth
Confidence and Trust
With SureCTMS and our suite of unified applications, network and platform, you’ll be able to source key clinical data with confidence. Our centralized, single data model ensures consistent clinical data availability for all SureClinical system users globally.
Flexible Clinical Project Budgeting
A critical part of effective clinical study management is the ability to create and manage study and project budgets. SureCTMS provides the ability to create multi-currency budgets for sites, vendors and organizations. Automatically track and report payments made and payments due for sites, study subjects, vendors, and organizations against your budget. Report on payments made, payments due and other finance tasks. Export payment vouchers with a broad range of external financial applications and payment gateways for payment completion and accounting.
Global Study Finance Management
Clinical trials are often conducted on a global basis. When sites, vendors and consultants are located in in multiple countries, it’s critically important to have multiple currency support for budgets, payment tracking and reporting. SureCTMS provides integrated multi-currency support for budgets, site payables, subject procedures, subject visits and many other financial activities.
Enable Better Decision Making
Start your day with a role-based dashboard project status view. With SureClinical operational intelligence, you can quickly determine tasks that are on track and areas that may need your attention.
SureCTMS provides a global status view of all projects. Each project has its own configurable dashboard and metric gadgets with the ability to drill down for details in context.
Metrics that Matter
View KPIs, Cycle Times and More
What gets measured gets done – We make it easy to see the status of your study KPI’s, cycle times and metrics. SureCTMS offers a dedicated Metrics tab that comes preconfigured with the most common metrics for study, site and clinical trial projects. Optimize your metrics dashboard with one click to add your own KPI’s and metrics. Easily configure dashboards with drag and drop metric gadgets.
Share Project Status
SureCTMS includes a wide range of project status, enrollment site activation and 20+ additional standard reports to keep your team informed.
Reports can be delivered on a subscription basis in both PDF and XLS formats. It’s easy to create your own custom reports, report subscription groups and custom notifications.
Configurable Reports and Notifications
SureClinical’s reports are user-configurable for both data and layout. Our easy to use report wizard allows users to quickly create, save, run and share reports tailored to their specific needs. Customized reports can be saved by users as templates that can be shared. Reports can be delivered on a subscription basis at configurable intervals.
The Fastest Path to Success
Customers and Users
"Our users, sponsors, and investigators are delighted by SureClinical’s suite of eClinical applications, including SureCTMS, SureETMF, and SureDrive."Gary ZammitCEO of Clinilabs Drug Development Corporation
"Of all of the systems I use, SureClinical is the best Clinical Trial Management Software."Deana DowdCRA Consultant, First Coast Clinical Research
“With SureClinical, we cut our clinical trial project startup time in half. Going digital was not only a significant time saver, but it also enhanced the quality of our data.”Global CRO
"With SureClinical eTMF Cloud, internal and external study stakeholders can collaboratively complete, digitally sign and share regulatory and study information in the cloud from mobile or web. This strategic capability allows us to eliminate paper at point of origin, accelerating document completion and enhancing document quality."Lynda ShelleyExecutive Director of Clinical Operations, Novotech
”With SureClinical, our goals of going digital have been met. We tested and sandboxed many systems before making the decision to go with SureClinical for SureETMF and SureCTMS. Our own client users are passionate about the software and it is incredibly easy to initiate, file and manage documents and trials."Global CRO