IMPROVE PROTOCOL COMPLIANCE IN CLINICAL TRIALS BY 95%
REDUCE STUDY DROPOUT RATES BY OVER 90%

87% OF PATIENTS WANT TO BE PART OF A CLINICAL TRIAL

70% OF PATIENTS LIVE AT LEAST 2 HOURS FROM THEIR NEAREST SITE

DELIVERING CLINICAL TRIALS TO PATIENTS WHEREVER THEY ARE

OUR MISSION IS TO IMPROVE PATIENT EXPERIENCE IN CLINICAL TRIALS

WE ENGAGE, CONNECT AND HELP IMPROVE QUALITY MEASURES
Unlock the power of decentralized clinical trials using the industry's leading web, mobile and SMS platform

STARTING AT $30/mo PER PATIENT
CLICK HERE TO SCHEDULE A DEMO

Patient Reported Outcome

Electronic Consent

Scheduled & Event Diaries

Medication & Visit Notification

RemoteLY Engage & Televisit

Delve Health Announces the Addition of TeleVisit to Clinical StudyPal - Enabling Patient-Centric Clinical Trials




















Delve Health Joins xCures and Cancer Commons to Support the Beat19 Data Initiative to Conquer COVID-19

virtual clinical trials

OUR DIGITAL PRODUCTS ARE DESIGNED TO Remotely Engage Patients And Collect Patient Outcomes Data Using multi-modals

Web, SMS And Mobile Platform

Patient

Recruitment

75% of patients that can be part of clinical research are simply not aware of the potential a clinical trial can bring to them. Together, we can bring awareness the benefits of your clinical trial, helping patients receive the treatments they need.

clinical trial patient recruitment
virtual clinical trials

CONNECT PATIENT WITH INVESTIGATOR

53% of patients find out about clinical trials through social media. Our dedicated team can help you develop a brand, a study website and a mobile app for your clinical trial that can reach the target patient audience on the go. We marry that with “multi-channel” advertising to help you meet your recruitment goals and connect patients to their nearest sites.



INVESTIGATOR PRE-QUALIFICATION

Investigator can pre-qualify the patient through a set of questions that automatically can help identify recruitment, and assess reason behind screen failures

patient pre-qualification
eConsent

eCONSENT

Empower patients to review study material and provide consent
electronically. Using web and mobile technology to remotely provide clear and easy-to-understand clinical trial information so that they are truly informed when making a decision to participate, and ultimately improve compliance.

SMS NOTIFICATION &

REMINDERS

Engaging patients wherever they are for

  • Medication or treatment Adherence
  • Upcoming visit/event notification
  • Push study notification and newsletter
epro patient reported outcomes
Patient Reported Outcomes

COLLECT eCOA

Using hybrid model of BYOD and/or provide supported devices to to allow patients, clinicians and caregivers to directly report outcomes, resulting in more granular endpoint data. eCOA measures include ePRO, ePerfO, eClinRO and eObsRO

electronic patient diary

INTEGRATE WITH WEARABLES AND REMOTE DATA SERVICES

Integrate wearables and other data services to Clinical StudyPal to remotely monitor parallel progress

wearable integration in clinical trials
Remote patient engagement

TELEVISIT

  • Well over 1,000 current studies are stalled by the COVID-19 Pandemic
    causing FDA Guidance which allows replacing site visits with virtual visits
  • Enhance patient safety through continuous patient feedback
  • Provide real time phone and video communication with patients and their caregivers on condition and any changes that need to be made to the study schedule and protocol resulting from COVID-19
  • 70% of patients live ≥2 hours from their nearest site, why not enable virtual visits for your upcoming studies?

Custom Applicaitons

Have a new idea to engage patients? We can help you ideate, design and test your concept

Develop Vision

We help understand and define the vision

  • Identify the pain, the market and value to users
  • Conduct user interviews to solve real problems
  • Develop product pitch deck

UX design

Help define the vision

  • Create actionable screens
  • Develop mock-ups that users can speak to
  • Define outcomes and results

Create Roadmap

Define the product roadmap based on the value

  • Work across stakeholders to create a value added roadmap
  • Partner with IT, marketing and sales
  • Define a commercialization output

Data Management

End to end data management capabilities, including database development, integration and data analytics

Data Management

Complete services, providing;

  • CRF design
  • Database design (Inform, Rave, Clindex, Clinical Studio)
  • Data validation and verification

Clinical Programming

Providing support for

  • CDISC, ADaM and SDTM datasets
  • Development of clinical study report
  • Interim & final analysis and data reconciliation

Reports and Analysis

Providing support for

  • Create reports across EDC/CTMS and Safety
  • Development of migration strategy
  • Drug and industry analysis

Why Choose Us

US Company

More than 20 years of enabling clients to improve clinical research outcomes through web, mobile and related services

Study Experience

Our team has managed, designed and executed over 300 studies across multiple disease states.

Team

We only employ the best. A team of organized and experienced analysts, programmers and MDs.

Technology

Our founding team has designed numerous applications with deep life science knowledge.

On Time Delivery

With over 300 studies across 10 solutions, we understand that each project is unique.

Compilance

We work with our clients to ensure data safety & compliance across all phases of any project.

Analytics

Let our team help you identify top identifying analytics that best fit your situation.

Clinical Solutions

Over 20 years of experience across multiple solutions to help you achieve the best results.

Our Blogs

Contact With Us

We can help you save money, increase productivity, provide seamless collaboration and help you save lives.

Request A Meeting