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    The Zelta way on AI

    Letting the use case decide on supervised machine learning and Generative AI. Download the whitepaper

    VISION

    Providing dynamic solutions that drive bold research

    Clinical research is getting more complex. Each study has its own unique needs and the investments in these trials are becoming more costly. There needs to be a better way to solve these challenges. 

    Zelta, a cloud-based unified clinical data management and acquisition platform with customizable modules, can be tailored to the meet the unique needs of your clinical trials -- providing more control and confidence over your trial outcomes. 

    Learn more about the platform

    500+

    PHASE III TRIALS

    Flexibility and scalability

    Manage clinical studies and research across all phases, therapeutic areas, levels of complexity and regions.

    Easy to use

    Execute research, manage participants, and report results to stakeholders from a single, user-friendly interface.

    Seamless access

    Use a single sign-on from anywhere in the world to access a unified solution built on one code base.

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    Video

    Building studies with complex dynamics in 1 week

    Rob Sandefur, former Principal Clinical Database Programmer for Lexitas Pharma Services, shares how Zelta has empowered his team to build clinical trial studies encompassing complex dynamics in as quickly as one to two weeks.
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    WHAT YOU GET

    Confidence in every outcome

    Access features tailored to support the clinical data management needs of contract research organizations, medical device companies, pharmaceutical companies, and academic research organizations, from start up to submission.
    Watch the video
    • Electronic data capture
    • CDM with AI-assisted study design
    • Reporting and analytics
    • Data integration
    • Query management
    • Monitoring

    WHAT YOU CHOOSE

    Control in every stage

    Maximize patient, caregiver, and provider engagement by choosing only what you need from fully integrated modules that help accelerate outcomes for that particular study, regardless of the number of participants, level of complexity, or stage.
    Zelta chosen for over 4,300 clinical trials

    Clinical Data management and acquisition

    • Electronic data capture
    • Medical coding with AI
    • Local labs
    Learn more

    Clinical operations

    • RTSM
    • Globalization
    • eLearning
    • Endpoint adjudication
    • CTMS (powered by BSI)
    • eTMF (powered by BSI)
    Discover

    Patient and provider engagement

    • eCOA/ePRO
    • eConsent
    Explore
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    YOUR STUDY, YOUR WAY

    Don’t settle for one-size fits all

    • Dial in your costs to align with the goals of your specific study by selecting what you need at the study level.
    • Choose the pricing model that works best for you — subscription or pay per use.
    • Control your study independently through self-service or use our best-in-class support services when you need it.
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    ACCELERATE YOUR TRIALS

    Don’t let your platform slow you down

    • Get the features and functionality you need on a unified cloud-based SaaS platform with a single code base.
    • Maximize efficiency with an intuitive interface.
    • Access from anywhere in the world with the convenience of single sign-on.
    Read: How SaaS breaks the mold for clinical trials
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    TRUST YOUR TECHNOLOGY

    Reliable, industry-leading solutions

    • Mix solutions from Zelta and our ecosystem partners with plug and play APIs to create a true configurable solution.
    • Protect your data by using a unified, compliant platform that is hosted on a secure and flexible HIPAA-enabled cloud.
    • Call upon certified, experienced designers for support 24/7/365.
    Zelta enables self-service support

    Ready to talk?

    Chat now

    “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

    Explore all case studies

    “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

    Explore all case studies

    “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

    Explore all case studies

    “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

    Explore all case studies
      30%

      Reduction in data management costs

      Read the Veristat story
      30

      Minutes to perform a minor study change and fully document the customer’s approval

      Read the ProTrials case study
      2

      Weeks to build their first study on Zelta

      Read the Alira Health story

      SERVICES

      Benefit from our expertise

      Human-centric

      People-first advisory services to help fully enable your business, including:

      • Cycle time benchmarking
      • Decentralized clinical trial readiness
      • Clinical operations planning
      Learn more

      Support

      Support to onboard your team and enable optimized adoption and usage through:

      • Implementation and integration
      • Training
      • Mentored build
      • Global 24/7/365 support

      Extension

      Additional services that extend and scale platform capabilities as your projects demand, including:

      • Study build
      • Templates
      • Advance Reporting

      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.

      What are the pricing options?

      No two companies are alike, and each clinical trial is different so our pricing options offer you flexibility and control.
      The subscription option can offer cost savings to larger organizations and those who need a predictable budget. Most modules are included without incurring additional fees and you may be eligible for volume discounts.

      The pay-per-use option is for companies who need flexibility without a long-term contractual commitment. There is transparent ala cart pricing, no minimums and fees start when the trial goes live.

      For specific pricing information, please contact us and one of our representatives can provide a customized quote based on your specific business needs.

      What services does Zelta offer?

      Customers have the option to use our consulting, support and enablement, and extension services. These include advisory services such as cycle-time benchmarking, decentralized clinical trial readiness and clinical operations planning; onboarding, including implementation and integration, training, mentored build and global support 24/7/365; and services that extend the capabilities of your business on our solutions including study builds, templates and smart reports.

      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.

      Ready to talk?

      See how we can meet your clinical development needs.

      Speak to sales
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