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Mahalo EDC

You collect data from actual human participants who want the most effortless process to provide you with the clean data needed for your study. Mahalo’s EDC system offers an intuitive Read More...
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SecuTrial EDC

In addition to data capture using electronic case report forms (eCRF), secuTrial® offers users the facility to create their own eCRFs without any programming knowledge. In addition to data capture Read More...
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Agatha QMS

Agatha Quality (QMS) is a complete, ready-to-use quality management application for capturing deviations, documenting corrective and preventive actions (CAPAs), and managing change control processes during a clinical research project. Most Read More...
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IQVIA Clinical Analytics

IQVIA Clinical Analytics Solutions (CDAS) helps you solve key challenges such as oversight, data management and clinical trials process automation. CDAS uses modern technologies to consolidate data, accelerate review, and Read More...
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Evident IQ eConsent

EvidentIQ eConsent improves trial participants experience by meeting them where they are. It enables the improved quality and efficiency of clinical trials through insight into the patient experience, improved data Read More...
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Clinevo eISF

Clinevo electronic Investigator Site File (eISF) is a cloud based, easy-to-use and highly secured electronic document management platform for investigator sites involved in the clinical trial for full control over Read More...
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Delve Health DCT

Clinical StudyPal’s DCT service automates the patient enrollment process, on-boarding patients more efficiently—securely and ethically. Delve Health offers a comprehensive suite of decentralized clinical trial (DCT) services designed to make Read More...
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Greenlight Guru ePRO

Empower and Engage Your Patients. Collect clinical outcome data via email/SMS and empower subjects to complete anytime, anywhere – on any device. Collect outcome data in-person, remotely, or with a Read More...
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Icon DCT

Decentralised clinical trials improve patient recruitment, retention and diversity, by putting the patient at the centre of clinical trial design. Every study must be evaluated for its suitability and requires Read More...
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Mednet eConsent

iMednet’s Electronic Informed Consent (eConsent) was developed within the iMednet platform to seamlessly integrate, ensuring a secure, simple and efficient electronic consent process for both study participants and site users Read More...
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betterclinical showcases over 400 clinical trial software

For an infographic representation of all these software solutions, have a look at the Clinical Trial Software Landscape.

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