SERVICES

The All-in-
One
Solution.

A CRO that delivers everything you need to run a study start to finish. All underpinned by our risk sharing business model; fixed upfront quotes for your entire clinical study, payable upon hitting pre-agreed milestones.

SERVICES

The All-in-
One
Solution.

A CRO that delivers everything you need to run a study start to finish. All underpinned by our risk sharing business model; fixed upfront quotes for your entire clinical study, payable upon hitting pre-agreed milestones.

WHAT DOES IT INCLUDE?

Our All-in-One CRO solution delivers the full package of CRO services, site operations and technology necessary to operate a study. It starts with building your protocol through to delivering your data.

01

Transparent
pricing

Aligned
incentives

03

Retaining
flexibility

02

Superior Customer experience

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Working with Lindus Health has been a game changer. We would love to work with them again and again!

- Mark Wuttke, CEO at Dopavision

"Working with Lindus has been a game changer. We would love to work with them again and again!"

- Mark wuttke, ceo at dopavision

CRO services

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Supporting your entire clinical trial journey from protocol writing and patient recruitment to data delivery

Study Startup
Patient RecruitmentData CollectionData Delivery

  • Protocol writing

  • EMR databank querying

  • Project management

  • Database locks

  • Site feasibility, selection, training and initiation

  • Central digital advertising campaigns

  • Data management

  • Interim data delivery

  • IRB submissions

  • On-site patient recruitment

  • Monitoring

  • Data standardization

  • Study configuration and UAT

  • Study websites and marketing materials

  • IMP logistics

  • Biostats and Programing

  • Study plans

  • Patient concierge

  • Vendor management

  • CSR writing

  • QA assurance


  • ISF management

  • Medical writing



  • TMF managment




  • Pharmacovigilance

Clinical site
Services

Depending on your study model we have the right site partnerships and staff to execute your study.

CONTACT

Clinical software platform

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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.

Our Unique Approach to Clinical Trial Technology

Patient Care and Engagement

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.

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01

Multi-channel enrollment features

Participant care management capability

03

Unified participant records enabling dedicated attention

02

High Data Quality

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.

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01

Machine learning assisted monitoring

Comprehensive issue monitoring

03

Automated data assurance systems

02

Efficient Close Out

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.

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01

Unified data pipelines

Automated data management

03

CDISC formatted direct data exports

02

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Ready to enjoy working with your CRO?

Let’s deliver better clinical trials together to get new treatments to patients faster.