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Clinical decision support

The Zelta way on AI

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

OVERVIEW

Control how you accelerate your clinical trials

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.

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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.
Rob-2

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 4,000 clinical trials

Clinical Data management and acquisition

  • Electronic data capture
  • Medical coding with AI
  • Local labs
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Clinical operations

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

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“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

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“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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    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

    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

    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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