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    Clinical decision support
    Clinical Data Management Platform

    Accelerate clinical trials. On your watch.

    Our no-code CDMS enables agile data management teams to independently design tailored studies and reduce build cycles by 2+ weeks.
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    Trusted globally by more than 200 biopharma, medical device, CRO and university institutions.

    4.6K+
    Trials launched, across all phases and stages
    500+
    Phase 3 trials launched
    1.3B+
    Clinical data points collected
    98%+
    Industry-leading CSAT scores

    Experience next-level efficiency with Zelta's Intelligent Study Design

    Break free from rigid workflows slowing you down.

    Automate weeks of manual database configuration

    Streamline study builds with Zelta’s advanced logic builder and the ability to easily reuse specific study objects from the current trial, previous trials or Zelta's library.

    Scale study operations without technical bottlenecks

    Our intuitive, no-code designer enables data managers to independently build studies and handle MSUs without over relying on vendor support.

    Tailor study set-ups to meet the most complex trial requirements

    Innovate with unrivaled flexibility. Create the study you need, leveraging our core EDC and a suite of connected modules. Enjoy seamless interoperability, powered by real-time AI-assisted edit checks.

    One, unified platform for all your clinical data needs

     

    Click through to explore the available modules within the Zelta CDMS

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    Case Study

    How Inventiv Matrix scaled from zero to 14 studies in 18 months

    Read more

      SERVICES

      Benefit from our industry-award winning services team

      Advisory

      Expert consulting to help solve process and system bottlenecks

      • Improve efficiency across clinical database delivery
      • Deliver consistent, compliant databases at scale
      • Enable integrated, end‑to‑end clinical data flow
      • Turn database metrics into actionable insight

      Enablement

      Training to drive seamless Zelta adoption for designers, users, and patients

      • Build a real study in a facilitated session
      • Implementation support for new modules, functionality and tasks
      • Tailored training for specific roles
      • Free multi-client sessions and resources

      Delivery

      Zelta Study Build Services for execution support and resource flexibility

      • Get help with full or partial study builds
      • Improve study design, standardization and quality
      • On-demand flex capacity to close resource gaps

      Care

      Industry-leading support and issue-resolution

      • Global support services
      • 24/7/365 availability
      • Accessible via email, phone & text

      Partnership

      Dedicated account managers for continued customer success

      • Regular check-ins on study activity
      • Long-term client advocacy on product enhancements and process updates

      Ready to talk?

      Let's see how Zelta can help accelerate your clinical trial workflows.

      Get in touch

      “Being able to shave a couple of weeks off a trial’s schedule is huge for us. We save on costs, and it also leads to the quicker launch of a product, which is highly meaningful for those affected by diseases.”

      Executive Vice President of Global Operations, Veristat

      Explore all case studies

      “We were able to build our first study in Zelta in just two weeks... The time savings have been great for us and it has been really easy to navigate the system.”

      Director of Data Management, Alira Health

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      “Building cleaner databases within Zelta has been an intuitive process. The contrast in data cleanliness between a Zelta-designed database and the databases we inherited from other vendors has been night and day.”

      CEO, Integrated Therapeutic Solutions

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      “The studies we’re doing are focused on treatment duration over longer timelines. We’re confident that Zelta can provide the self-service support we need for these studies.”

      Chief Science Officer, Vogenx

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      “The Zelta support team is great. They get to us very quickly... with any support issues. If I'm having trouble going live or anything like that, they will immediately get back to me. The support is fantastic.”

      Chief Operating Officer for Fast-Track Drugs and Biologics

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        Zelta is a proud member of the following organizations:

        What is Zelta?

        Zelta is a unified clinical data management and acquisition platform with customizable modules that can be tailored to the unique needs of your clinical trials.

        It gives you full command of every aspect of your clinical trials and research — from designing workflows and forecasting costs to decentralized trials solutions that better reach your participants and providers. We empower you to take control in every stage and our solution is designed to help you accelerate trial outcomes with confidence.

        Why is a unified platform with one code base important?

        A unified platform enables you to access modules and reports from anywhere in the world with true single-sign on and one code base. This allows you to

        • Use single instance technology to ensure that all of your trials and users are on the latest version of code
        • Streamline clinical trial processes and help maximize patient, caregiver and provider engagement with integrated clinical operations and patient and provider modules.
        • integrate third party systems and monitoring through intuitive point-and-click data mapping

        Why do you offer modules individually rather than as a package with the core functionalities?

        We know that every trial is different, and you should have the option to only pay for what you need, when you need it. We give you the freedom to choose and easily integrate solutions from both Zelta and other technology vendors, creating a true configurable solution. We offer commercial options that let you pay only for what you consume at a study level or set up a “standard” configuration at the portfolio level.

        Can I use Zelta globally?

        Host and scale trials around the world with single sign on to a solution that enables you to maximize international site and patient engagement, supporting more than 70 languages and dialects.

        How does Zelta make the clinical development process easier?

        It is designed to give customers:

        • Direct control of study go-lives, protocol amendments, study design changes and study closeouts
        • A user-friendly interface that makes it easier to implement and execute research, manage participant compliance, perform routine tasks and report results to stakeholders.

        How many of the top 20 pharmaceutical companies work with you?

        All 20 of the top pharmaceutical companies have used Zelta.

        Is the platform secure?

        The Zelta platform is hosted on a secure and flexible HIPAA-enabled cloud. Our platform is planned, developed, deployed and supported consistent with ISO 9001:2015, ISO 27001:2022, ISO 27701:2019, ISO 27017:2015, ISO 27018:2019 and in compliance with 21 CFR Part 11 and data privacy regulations.