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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. To efficiently manage trials, organizations participating in clinical trials often utilize Clinical Trial Management Systems (CTMS) with an integrated Electronic Trial Master File (eTMF) to consolidate all their operational data. However, for some organizations, because of the cost and commitment required for most CTMS, it becomes a lower priority.

Easy, affordable eTMF integration

Clario eTMF is a new option that can get up and running quickly and efficiently. Built on the same platform as Clario CTMS and available with affordable add-on pricing, it maximizes value, minimizes headaches and meets all regulatory requirements, from support for the most recent DIA Reference Model to 21 CFR Part 11 compliance to a complete audit trail.

Available anytime, anywhere

Clario CTMS is an intuitive end-to-end clinical trials management solution that brings control, efficiency for both data flow and workflow, and quality data to every study, yielding cost savings in time, labor and operational expenses. This web-based CTMS works on the go, letting you view and manage real-time operational performance — wherever and whenever.

Familiar interface

With the Microsoft Office-based work environment, Clario CTMS transforms a disjointed clinical trial into an efficient and cohesive work environment using the most widely used office productivity tools in the world. Bi-directional information exchange from Clario CTMS to SharePoint and other Microsoft products is seamless, making for a powerful, high-performance solution. Moreover, integrating Office processes with clinical operations can reduce back-office paperwork, significantly lower administrative overhead and result in low total cost of ownership.

Rapid implementation

Easy to learn and use, Clario CTMS is quickly mastered, which speeds user adoption. It is mobility-enabled in support of the one-of-its-kind Monitoring Visit Report (MVR) module, allowing operational performance to be viewed and managed across programs and studies in real-time via secure role-based web access.

Our streamlined configuration process and standardized reporting package let companies get started with CTMS in as little as 2-3 weeks rather than the weeks or months of a traditional enterprise CTMS implementation.

Access a single, centralized source of truth across your studies

Full-featured

Standardized tracking
across all studies

Pay as you go pricing

How it works

Clario CTMS is Microsoft Office-Smart. It allows you to leverage the Microsoft Office suite (SharePoint, Outlook, Excel, Word, Access and Project) to access, update and report on study data, as well as track and manage study activities securely and compliantly.

Clario 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. Bi-directional information exchange between Clario and SharePoint and other Microsoft products is seamless, making for a powerful, high-performance solution. Document updates done in SharePoint are automatically reflected so that your trial data is accurate, current and in sync. And since most CTMS interaction is through familiar Microsoft applications, users work in a familiar interface, so the training is minimal, and the user adoption is high.

Clario CTMS connects the many moving parts of the clinical trial process and lets you monitor progress from a central dashboard. It 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: design, procedures, protocol, study arms, visits, forms, treatments, payments and more.

The robust core system offers a range of benefits for improved clinical trial efficiencies and operations:

  • Provides the right level of access with views tailored to individual users, whether internal or external
  • Provides maximum study visibility for informed decisions at all levels
  • Is an ideal governance tool for managing CROs and vendors (consolidates multiple reports/exports a variety of formats and timelines into a central system)
  • Supports studies of all types, sizes, phases and complexity in all therapeutic areas
  • Is built to demanding scalability specifications of top tier pharma, while providing a right-sized solution for any organization

Through automation, Clario creates vast improvements in workflow to improve the way teams work:

  • Logistical and operational data are centralized for streamlined management and enhanced control
  • Clinical operations and critical business processes across the trial lifecycle are aligned within the regulated environment
  • All the moving parts of global trials and various stakeholders are connected by removing communication barriers and facilitating collaboration
  • Automation for reviews and approvals ensures nothing slips through the cracks
  • Compliance and traceability ensure data and activities are auditable for accuracy and completeness
  • Original, modified and actual milestone dates can be tracked across studies, countries and clinical sites
  • Site monitors and study managers have one place to see data across all studies
  • Many users can access data for their specific needs
  • Streamlined dashboards provide the operations team with visibility into all clinical studies
  • Extensive standard and custom reports provide quick answers

Clario has a unique set of value-added capabilities that complement its robust core system and go above and beyond any other CTMS. This includes:

  • eTMF: Don’t have an existing eTMF solution? Add the new Clario eTMF to your CTMS for a low incremental cost and get everything you need, without the hassle — a fully compliant solution that meets regulatory requirements; a user-friendly SharePoint interface for streamlined adoption; seamless interaction with CTMS; and complete flexibility to migrate to another system if your needs change.
  • Monitoring Visit Report (MVR): Bi-directional data flow between Microsoft Word and Clario enables monitors to enter information with or without an internet connection. The MVR auto-populates report templates and updates the system automatically for significant time and labor cost savings. 2012 Microsoft Life Sciences Innovation Award winner, MVR.
  • ClinicalTrials.gov: Clario CTMS generates electronic submissions in the required format for clinicaltrials.gov.
  • Payment Module: The module dramatically shortens payment cycle times, automates invoicing and includes contract/budget management exchange rate accounting tools. It supports Sunshine Act Reporting compliance for cash transactions and enables study data to be easily combined with other payment information in an aggregate spend system.
  • Contact Management: Manage contacts and institutions to reflect multiple, real-world relationships of study personnel. Information is accessible in Outlook.
  • Extensive Standard Reports: Get instant operational visibility into Key Performance Indicators with real-time data and easy exports to both Excel and Adobe.
  • Robust Reporting and Tracking with Customer-Defined Milestones: Track original, modified and actual milestone dates across studies, regions and clinical sites. Visualize progress using SharePoint calendars and charts through MS Project integration.
  • Inventory Control Module: Tracks shipment and dispensing of general study supplies, equipment and test articles so that the location and product balance at each site is always known (e.g. lot numbers, expiration dates and reconciliation information).
  • Single Sign On (SSO): Claims-based security and authentication across Clario products simplifies the user experience.

CTMS demo video

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