Study Oversight

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Monitor all your clinical trial performance from startup to closeout

Study Oversight provides you with a single source of truth to monitor your clinical trial performance, compliance, and risk in real-time. Monitor trial progress from startup to closeout, ensuring a successful study outcome.

Operational Oversight Sample Screen
Real-time study health

Real-time study health

View all of your relevant study data in real-time through a consolidated dashboard that enables you to be up-to-date on milestones, study progress, and other KPIs.

Increased Confidence

Increased confidence

Mitigate research risks by identifying and addressing issues as they occur, radically improving trial performance.

Operational efficiency

Operational efficiency

Benchmark trial performance against Lokavant’s proprietary data to optimize your resources and reduce study team burden.

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Study Oversight helps improve trial performance and mitigate trial risks in real-time

The right data at the right time

In a global, Phase II, multi-center study, Lokavant helped a biotech combine 18 source systems into 1 comprehensive study dashboard with ability to scale long-term across their portfolio.

Data aggregation
& harmonization

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Trial data from source is ingested and harmonized in real-time with Lokavant’s proprietary and partner data

Central dashboard for all
study reporting

Central dashboard for all study reporting

A single, self-service view of real-time study performance with automated reporting and benchmarking

Predictive enrollment
forecasting & risk

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Daily reforecasting of enrollment and site performance is compared against historical performance to provide actionable insights

Features

Connected dashboards View all your study operational data through a connected dashboards that eliminates the need for time-consuming manual data aggregation.
Compliance Ensure compliance with 21 CFR Part 11, and ICH E6 (R2), ensuring your clinical trial data are reliable and secure for regulatory submissions and clinical decision-making.
Real-time
data comparison		 Determine where your study plan needs improvement and see your combined study data in real time to dig down into country, site, and subject level views.
Configurable Gain complete control over your research data without compromising security. Turn on-off features and adjust the level of access to customize the dashboards to your specific needs.
Risk transparency Evaluate study indicators with a color-coded performance system to identify critical risk areas and quickly assess the trial’s progress according to plan.

 

Why Lokavant

Lokavant’s Clinical Trial Intelligence platform offers clinical researchers and study teams solutions to predict trial performance. Leveraging our Clinical Data Hub with over 21+ source connectors and proprietary data from over 2000+ harmonized trials and 14,000+ 3rd party trials, Lokavant can help you design, plan and execute trials more efficiently and give you the confidence to make informed decisions.

Featured Resources

Analytics in DCT & Hybrid Trials

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Lokavant partnered with THREAD to conduct the first ever impact analysis of DCTs on key performance indicators during the pandemic.

Predictive Enrollment

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Learn how to predict key enrollment outcomes earlier in a study’s trajectory and with 95% accuracy.

Participant Discontinuation

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Expert analysis that investigates the key predictive factors that increase and decrease risk of participant discontinuation.

Sponsors and CRO’s love us

Parexel
CMIC
Enzyvant
Roivant
Ergomed
Eloxx
Thread
Sumitomo

Get in touch

Schedule a demo to learn how Lokavant can transform your clinical trials.