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Lindus Health launches industry's first Diagnostics CRO offering.
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Supporting your entire clinical trial journey from protocol writing and patient recruitment to data delivery
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Supporting your entire clinical trial journey from protocol writing and patient recruitment to data delivery.
AI-assissted trial design
Protocol writing
Site feasibility, selection, training and initiaiton
IRB/ethics and regulatory submissions
CTMS configuration and UAT
Study plans
EMR databank querying
Central digital advertising
On-site patient recruitment
Study websites and marketing materials
Patient concierge
Pre-screening
Project management
Monitoring
Vendor management (e.g. IMP, central lab, IRT etc.)
TMF managment
Pharmacovigilance
Medical monitoring
Database locks
Data delivery in CDISC SDTM format
Data standardization
Biostatistics and Programing
Medical writing
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And to make everything even smoother, our end-to-end technology platform covers all your clinical software and tool needs. Our technology supercharges studies to deliver faster study startups and recruitment timelines.
No need to stitch together multiple data tools. Our Citrus platform provides all essential data capture, management, and delivery tools you are accustomed to, but with greater efficiency and speed to capture and deliver data in one seamless platform.
Speed to full recruitment is an enduring challenge for the industry. Lindus Health solves recruitment via it’s integrated approach. Poor patient engagement is a top reason for poor quality data and withdrawals.
Our software platform focuses on dramatically increasing retention and completion rates via workflow tools for study teams to deliver exceptional care to patients from first contact to close out.
Keeping up with high complexity of trial data constitutes a large portion of excess CRO costs. Traditional monitoring methods that rely heavily on on-site visits are a relic of the past.
Centralized monitoring is today’s norm, but we take it a step further by integrating all capabilities in a single platform. This gives sponsors instant access to a unified datastream.
Instant access to data allows us flexibility and freedom to build guardrails around clinical data, leading to significantly reduced protocol deviations and queries. We avoid the need for data cleaning by ensuring data we collect is clean.
Conventional approaches to trial delivery and most technology solutions utilize a multitude of vendor solutions with disconnected systems. Study teams struggle to connect the dots and put together submission ready datasets.Our end to end technology platform makes it trivial to reconcile all study data and pull the final dataset from a single system. Database lock and handover is conducted instantly to move along to regulatory submission. Burden to close a trial is not impacted by higher study complexity. Our unified data stream eliminates the typical pains of transferring data between, Source, EDC, and delivery in CDISC.
Let’s deliver better clinical trials together to get new treatments to patients faster.
