Lindus Health launches Womens Health 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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"Lindus goes above and beyond to help tackle unexpected changes as they arise and provide exceptional services every step of the way.”
“In the past I’ve felt like most my interaction with CROs was about change orders; having a real partner with cost certainty is a game changer.”
“Working with Lindus has been a transformational experience. We would love to work with them again and again!”
"Lindus Health’s approach to clinical trial execution and their associated technologies should be incredibly helpful to biotech and pharmaceutical companies and enable them to bring new therapies to market faster and more efficiently."
“Working with the Lindus Health team has forever changed our experience running clinical trials. They have a can-do attitude and make things happen, going above and beyond the call of duty.”
“Lindus puts great emphasis on aligning incentives with sponsors, and their risk-sharing, milestone-based payment model is much needed in the CRO industry. Their patient and technology-centric approach to clinical trials will greatly benefit biotech and pharma companies, enabling faster, cost-effectve studies.”
"Lindus goes above and beyond to help tackle unexpected changes as they arise and provide exceptional services every step of the way.”
“In the past I’ve felt like most my interaction with CROs was about change orders; having a real partner with cost certainty is a game changer.”
“Working with Lindus has been a transformational experience. We would love to work with them again and again!”
“Working with the Lindus Health team has forever changed our experience running clinical trials. They have a can-do attitude and make things happen, going above and beyond the call of duty.”
"Lindus Health’s approach to clinical trial execution and their associated technologies should be incredibly helpful to biotech and pharmaceutical companies and enable them to bring new therapies to market faster and more efficiently."
“Lindus puts great emphasis on aligning incentives with sponsors, and their risk-sharing, milestone-based payment model is much needed in he CRO industry. Their patient and technology-centric approach to clinical trials will greatly benefit biotech and pharma companies, enabling faster, cost-effectve studies.”
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.
