Simplifies & Optimizes Clinical Trials Workflow Ecosystem
COSMOS is for everyone
Site
Sites can sign-up for free to acquire new study leads, share the site and investigator profile with the sponsor and cro’s
Sponsor / CRO
Identifies experienced investigators & sites, Part II compliant CDAs process, feasibility, and locates CRAs, Regulatory specialists.
CRA/Regulatory/CRC
By registering with Cosmos, you'll gain increased visibility among site, sponsors and CROs. It's completely free, and there's no obligation to use.
Solutions for Sites
COSMOS is developing a clinical trial echo system to unite sponsors, clinical trial sites, and regulatory agencies on a one platform. Sites can sign-up for free to acquire new study leads and subscription required to use the next generation CTMS, eRegulatory, eSource, eDairy, etc. features.
Solutions for Sponsors / CRO’s
COSMOS offers strategic advice, identifies excellent sites, completes CDAs, clinical trial feasibility, and locates CRAs, study intelligence, and operational assistance for clinical research projects all over the world.
Why Choose Us
Clinical trials echo system, Cosmos is designed to execute worldwide clinical trials from site identification to archiving research documentation end-to-end. Organization for clinical research and the registration of medical devices and pharmaceuticals around the world.
The Cosmos clinical research and development echo system offers strategic assistance for clinical development across the world. Sponsors and contract research organizations (CROs) can use our web platform to discover clinical trial locations, sign a confidentiality agreement, and check the viability of each site with hundreds of researchers across the world.
Clinical trial locations, investigators, regulatory professionals, clinical research associates, and other service providers may all be found through Cosmos, which offers access to them from across the world.
The Cosmos clinical research and development echo system offers strategic assistance for clinical development across the world. Sponsors and contract research organizations (CROs) can use our web platform to discover clinical trial locations, sign a confidentiality agreement, and check the viability of each site with hundreds of researchers across the world.
Clinical trial locations, investigators, regulatory professionals, clinical research associates, and other service providers may all be found through Cosmos, which offers access to them from across the world.
Site Explorer
Search cosmos vast site database by region, therapeutic areas to identify the potential sites for a study from across the world
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Site Feasibility
Clinical trial feasibility is the process of determining the likelihood of conducting a specific clinical trial in a specific geographical region
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CTMS
COSMOS CTMS enables you to overcome the difficulties of traditional clinical trial methods
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eDocs
Don't limit yourself to a binder. Using a system built for site and sponsors with a significant number of protocols will save you time.
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eSource
For your clinical trial team, processing paper forms might provide several challenges, such as increased work hours and a higher chance of mistake
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eLabs
The Cosmos clinical document folder receives all the test results, images, medical records, and EKGs
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eCOA/ePRO
Cosmos is the only place you'll find this unusual feature. Instead of utilizing a paper diary, the site may construct an eDiary and schedule it for the research volunteers
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Digital Budget
COSMOS enables clinical trial sponsors, CROs, and sites to improve on their budget build and optimize their Study Start-Up process by relying on an exclusive clinical trials echo system platform.
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Resource Explorer
Our goal at COSMOS is to develop a global clinical study echo system. CRAs and regulatory specialists can register for free on the platform
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Digital CTA
A considerable number of Study Start-Up delays are associated with challenges related to budgeting and negotiation. COSMOS simplifies the process and allows for streamlining the budget and negotiation process to finalize the CTA execution through various enlisted capabilities.
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TeleVisit
In today's remote and digitized world, the human element is more imperative than ever. Our solutions provide a secure and highly interactive experience for complex, inbuilt e-signature, rich collaboration features, and web-enabled videoconferencing to allow you to transact and engage as humanely as possible.
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eConsent
COSMOS eConsent transforms the conventional patient consent approach by making the entire process easy, truly patient-centric, and improving transparency. It is designed for decentralized, virtual, and hybrid research projects to help deliver compliant, patient-centric, and site-friendly experiences.
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eSafety also offers a more efficient way of addressing patient safety while staying compliant with the study regulatory requirements. COSMOS eSafety is a single platform with multiple tools you need to run your clinical study successfully.
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EOS Data Exchange
eVault utilizes COSMOS seamless integration to facilitate the secure and automated transfer of EOS data from EDC, IWRS, eCOA, etc., systems and electronically collect the site's acknowledgment.
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DCT
Despite the uncertainty and challenges associated with the centralized to the decentralized clinical trials transition process, we are devoted to accompanying research sites in their digital transformation journey.
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