How Lokavant serves Sponsors

We partner with Sponsors to accelerate the development process with flawless clinical trials.

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Better oversight to ensure the best outcomes.

Identify and amend potential system issues in your study documents and databases early, and prevent errors from compounding later in the study.

Make more informed decisions on site startup and reactivation trajectories by benchmarking KRIs, especially in COVID-impacted environments.

Ensure patient safety through real time PD, AE, and SAE tracking and alerts.

Reduce unnecessary reporting and data cycle times by seeing all of your studies in one place.

Effectively manage all third parties to ensure adherence to your budget and timelines.

Communicate effectively within Lokavant’s fully auditable platform by using notifications and permissioned views.

Lokavant In Action

Helping a sponsor deploy and scale during the height of COVID.

Key challenges

Monitoring new, complex EDC data sources

Key data for safety and efficacy endpoints were being captured through novel direct data capture from ICU.

Condensed timelines

FPFV in less than 40 days

High stakes pivotal study

Data compliance and quality paramount

Rapid scale

Study expected to expand to dozens of sites.

Lokavant Solution

Harmonized EDC and direct-data sources for real-time access and analytics, instantly revealing data quality issues

Accelerated deployment to meet sponsor’s needs

Date pipeline fully compliant with GXP and 21 CFR part 11 within accelerated deployment timeline to ensure data quality.

Trial scaled to over 20 sites with Lokavant used across all sites

Get in touch

Schedule a demo and consultation to learn more how Lokavant can transform your trials.

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