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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'S INCLUDED

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

Always get
the “A Team"

02

CRO services

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

Study Startup	Patient Recruitment	Data Collection	Data 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

What is it like to work with Lindus?

"Lindus goes above and beyond to help tackle unexpected changes as they arise and provide exceptional services every step of the way.”

James Dacombe

CEO at CoMind

“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.”

Dr. Stephen Deacon

CSO at Pharmanovia

“Working with Lindus has been a transformational experience. We would love to work with them again and again!”

Mark Wuttke

CEO, DOPAVISION

"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."

Dr. Robert Langer

Founder, Moderna, 40+ Biotech companies

“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.”

Akash Bijlani

Director, Global Market Access at Aptar Pharma

“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.”

Dr. Tim Garnett

Former CMO, Eli Lilly

"Lindus goes above and beyond to help tackle unexpected changes as they arise and provide exceptional services every step of the way.”

James Dacombe

CEO at CoMind

“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.”

Dr. Stephen Deacon

CSO at Pharmanovia

“Working with Lindus has been a transformational experience. We would love to work with them again and again!”

Mark Wuttke

CEO, DOPAVISION

“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.”

Akash Bijlani

Director, Global Market Access at Aptar Pharma

"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."

Dr. Robert Langer

Founder, Moderna, 40+ Biotech companies

“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.”

Dr. Tim Garnett

Former CMO, Eli Lilly

Protocol writing
Site feasibility, selection, training and initiation
IRB submissions
Study configuration and UAT
Study plans

Patient Recruitment

EMR databank querying
‍
Central digital advertising campaigns
On-site patient recruitment
Study websites and marketing materials
Patient concierge

Data Collection

Project managment
Data management
Monitoring
IMP logistics
Vendor management
ISF management
TMF management

Database locks
Interim data delivery
Data standardization
Biostats and Programing
CSR writing

CRO Services

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

Study Startup

AI-assisted trial design

Protocol writing

Site feasibility, selection, training and initiaiton

IRB/ethics and regulatory submissions

CTMS configuration and UAT

Study plans

Patient Recruitment

EMR databank querying

Central digital advertising

On-site patient recruitment

Study websites and marketing materials

Patient concierge

Pre-screening

Study Management

Project management

Monitoring

Vendor management (e.g. IMP, central lab, IRT etc.)

TMF management

Pharmacovigilance

Medical monitoring

Data Management

Database locks

Data delivery in CDISC SDTM format

Data standardization

Biostatistics and Programming

Medical writing

Demo

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Free

Forever!

Starter

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$14.99

/mo billed annualy

Professional

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$24.99

/mo billed annualy

Agency

Lorem ipsum dolor sit amet, consectetur adipiscing elit. Suspendisse varius enim in eros elementum tristique.

$34.99

/mo billed annualy

Demo

Lorem ipsum dolor sit amet, consectetur adipiscing elit. Suspendisse varius enim in eros elementum tristique.

Free

Forever!

Starter

Lorem ipsum dolor sit amet, consectetur adipiscing elit. Suspendisse varius enim in eros elementum tristique.

$14.99

/mo billed annualy

Professional

Lorem ipsum dolor sit amet, consectetur adipiscing elit. Suspendisse varius enim in eros elementum tristique.

$24.99

/mo billed annualy

Agency

Lorem ipsum dolor sit amet, consectetur adipiscing elit. Suspendisse varius enim in eros elementum tristique.

$34.99

/mo billed annualy

What is it like to work with Lindus?

"Lindus goes above and beyond to help tackle unexpected changes as they arise and provide exceptional services every step of the way.”

James Dacombe

CEO at CoMind

“In the past I’ve felt like most of my interactions with CROs were about change orders; having a real partner with cost certainty is a game changer.”

Dr. Stephen Deacon

CSO at Pharmanovia

“Working with Lindus has been a transformational experience. We would love to work with them again and again!”

Mark Wuttke

CEO, DOPAVISION

“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.”

Akash Bijlani

Director, Global Market Access at Aptar Pharma

"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."

Dr. Robert Langer

Founder, Moderna, 40+ Biotech companies

“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-effective studies.”

Dr. Tim Garnett

Former CMO, Eli Lilly

“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.”

Dr. Stephen Deacon

CSO at Pharmanovia

“Working with Lindus has been a transformational experience. We would love to work with them again and again!”

Mark Wuttke

CEO, DOPAVISION

“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.”

Akash Bijlani

Director, Global Market Access at Aptar Pharma

"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."

Dr. Robert Langer

Founder, Moderna, 40+ Biotech companies

“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-effective studies.”

Dr. Tim Garnett

Former CMO, Eli Lilly

SERVICES

Clinical Site Services

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

Cooking

Writing
Course

100
TOPICS

Writing

Writing
Course

100
TOPICS

Business

Business
Course

100
TOPICS

01

Traditional Sites

Academics, hospitals, research facilities and on-site Principal Investigators and Clinical Research Coordinators

No Delays

02

Community Sites and Networks

Local Primary Care Physician and GP Sites, Speciality Sites (Neurology, Dermatology, Endocrinology, etc.), Site Networks (Urgent care chains)

03

Virtual and Hybrid Sites

In-house virtual clinical research coordinators, virtual Principal Investigators, mobile phlebolotmy and nursing, and patient concierge.

SERVICES

Clinical Site Services

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

Traditional sites

Academics, hospitals, research facilities, on-site Principal Investigators and Clinical Research Coordinators

Community Sites and Networks

Local Primary Care Physician and GP Sites, Specialty Sites (Neurology, Dermatology, Endocinology, etc.), Site Networks (Urgent care chains)

Virtual and Hybrid Sites

In-house virtual clinical research coordinators, Virtual Principal Investigators, mobile phlebotomy and nursing, patient concierge

Services

Clinical software platform

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.

EDC - Electronic Data Capture

The only single stream of data from direct data capture, to source, to EDC that allows for CDISC exports in real-time.

Clinical Trial Management System

A trial management system that tracks all study activities with real-time dashboards to keep tabs on study progress.

Supports on-site, remote, one-party, and multi-party consent.

Participant Pre-screening

Automate pre-qualification of thousands of participants through easy online questionnaires.

Electronic patient reported outcomes and electronic clinical outcomes assessments of all kinds are supported.

Our platform’s direct data capture allows for a clear line of site sourceNotifications and Reminders - keep your patients and staff on track with customized nudges for the important things.

See patients virtually as well as in person.

Principal Investigator, Clinical Research Coordinator, and other site staff can easily manage their patients in one portal.

Safety database

Set up and manage AE and SAE workflows.

Visit Scheduling

Set up in-person and virtual appointments.

APPROACH

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.

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.

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.

01

Unified data pipelines

Automated data management

03

‍CDISC formatted direct data exports

02

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

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