Built with all users in mind, Clinical Development modules from Merative are fully integrated and share one code base for a truly unified platform. This streamlines clinical trial processes and helps you:

• Maximize patient, caregiver and provider engagement to accelerate clinical trial outcomes. 

• Control research of all types regardless of phase, therapeutic area or geographic location. 

• Easily implement and execute research, manage participant compliance, perform routine tasks and report results to stakeholders through a single, user-friendly interface. 

• Access modules and reports through a unified platform from anywhere in the world with single-sign on and one code base.

• Successfully enable complex research protocols and integrate decentralized trial solutions from fully virtual to hybrid designs. 

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

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 Merative 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. 

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 60 languages and dialects (and growing). 

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.

Yes Merative Clinical Development are being used for traditional, hybrid and decentralized clinical trials. Since 2018, the phases of studies managed by Merative Clinical Development can be broken down as follows:

23% Phase I

33% Phase II

16% Phase III

10% Phase IV

7% Post Market

5% Registry

5% Feasibility

All 20 of the top pharmaceutical companies have used Merative Clinical Development.

Medical device companies can eliminate managing and cross checking multiple external systems with the full-integrated DICOM capabilities in Merative Clinical Development. They can also take advantage of training, study builds and additional resources that can help you overcome common challenges in clinical trials whether it is MDR, 510k, or other medical device needs.

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. 

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. 

Merative Clinical Development is hosted on a secure and flexible HIPAA-enabled cloud. Our platform is planned, developed, deployed and supported consistent with  ISO 9001:2015  and in compliance with  21 CFR Part 11  and  data privacy  regulations.