Lokavant Description
View your study data in real time through a dashboard that allows you to stay up-to date on milestones, progress of the study, and other KRIs. Mitigate risks in research by identifying issues and addressing them as they arise, improving trial performance dramatically. Lokavant's proprietary trial data can be used to optimize resources and reduce the burden on study teams. Trial data is ingested from the source and harmonized with Lokavant proprietary data and data from partners in real-time. Self-service, single view of real-time performance of studies with automated reporting and benchmarking. Daily re-forecasting is used to compare enrollment and site performance against historical performance. This provides actionable insights.
Lokavant Alternatives
eDeviation
eDeviation supports all operations related to Protocol Deviation management and assessment. From software design and validation to gathering supporting documents and exporting data to the TMF, eDeviation®, relieves your clinical staff from the risks of missing or incorrectly assessing protocol deviations.
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AcceleTrial
AcceleTrial™, takes the guesswork out identifying and activating clinical trial sites. Our Study Start-up Management System is based on objective data, not self-identification. AcceleTrial™, a global database of thousands of sites, is indexed and ranked based on: Objective Site-specific Therapeutic Expertise and Objective Site-specific Clinical Test Experience. Objectively match the right sites with objective data on expertise, patient data, and experience to your clinical trials. AcceleTrial™, an automated "push-and-pull" structure, allows you to quickly launch the right sites and begin enrolling patients. It is available in multiple languages. Collect required documents accurately using pre-filled templates. Track activities in real time. You can immediately start using the system - a cloud-based solution that requires minimal IT setup or training. Integrate AcceleTrial™, CTMS, or other clinical trial system.
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Clario CTMS
Clario CTMS is a user-friendly, intuitive, end-to-end management system for clinical trials. It brings control, efficiency and quality to data flow and workflow. This results in cost savings in time and labor, as well as operational and operational expenses. This web-based CTMS allows you to view and manage your operational performance anywhere and anytime. Clario CTMS, a Microsoft Office-based workplace environment, transforms disjointed clinical trials into a cohesive and efficient work environment by using the most popular office productivity tools around the globe. Clario CTMS can seamlessly exchange information with SharePoint and other Microsoft products. This makes it a powerful, high-performance system. Integrating Office processes with clinical operations can reduce paperwork, significantly lower administrative overhead, and result in a low total cost of ownership.
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Clinion eCOA
Clinion eCOA allows you to conduct decentralised clinical trials, with patients participating remotely.
Clinion eCOA allows study participant to report their health from their home using their smartphone. This allows clinicians to monitor patients in real time.
Clinion eCOA integrates seamlessly with Clinion EDC. Trial participants can input daily outcomes directly. This eliminates data duplication and transcription errors, and provides clinicians with a real time view of patient progress.
Multilingual forms are supported by the eCOA app, which makes it easier for patients to engage and provides cleaner data. The eCOA app's decentralised nature allows for faster and wider patient recruitment.
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Integrations
No Integrations at this time
Company Details
Company:
Lokavant
Website:
www.lokavant.com
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Product Details
Platforms
SaaS
Type of Training
Documentation
Live Online
Customer Support
Online
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