How it works

Signup as Site

Getting started is really a simple process. As a site you just need to fill in some basic information and then you are all set.

Add sites users

The next step after signup will be to add the users like Coordinators, Investigators, Research Assistants and your other staff to your clinical research center

Create Study

After you have added users you can start creating studies for your clinical trials.

Add/Import Patients

Once the study is created, now you can add or import subjects for your clinical trials

Let's get started

Efficiently manage your internal regulatory compliance process

For Patients & Families

Looking for a clinical trial or thinking of participating, orangectms is a great place to start

Patients Scheduling

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Patients Health Records

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Efficiently manage your internal regulatory compliance process

Audit Trail

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Financials

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Reporting

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Efficiently manage your internal regulatory compliance process

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Seamlessly run multicenter trials across the globe and capture high-quality, submission-ready data from patients and clinicians by leveraging our EDC, eCOA (including ePRO), EHR eSource, eConsent, and IRT modules. Reduce time-to-market for your medical devices by efficiently capturing and integrating data from multiple sources on the top-rated clinical data management system (CDMS). by leveraging our EDC, eCOA (including ePRO), EHR eSource, eConsent, and IRT modules. Reduce time-to-market for your medical devices by efficiently capturing and integrating data from multiple sources on the top-rated clinical data management system (CDMS).

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