Up to 90% better reported outcomes, remotely monitor patients and quickly address possible adverse events
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
Real-time notification to improve medication or treatment Adherence, Upcoming visit/event notification and notify investigators or sponsors of any adverse or safety issues
Increase patient recruitment through various digital avenues, including study website, mobile app and digital advertisement agencies to gain a bigger pool of patients
Real-time phone and video communication for clinical trials. Enhance patient safety through continuous feedback, and allowing clinical trials to keep moving forward.
Investigator can pre-qualify the patient through a set of questions that automatically can help identify recruitment and assess reason behind screen failure
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.
Utilizing at home nurses to help improve patient retention, lower patient risk and make it easier for patients to be part of clinical trials. We understand that every clinical trial is different. Our experienced team will help you identify the right level of in-home services, and whether a nurse or phlebotomist is needed based on the protocol design. We partner in-home nurses with our Clinical StudyPal to provide full transparency of the data collected at that visit, and ensure data compliance throughout the trial.
Delve Health understands the need to spearhead clinical trial advancements. This is why we use science, technology, and human science to make informed decisions about the present and the future.
Through this, we need a seamless process to merge the data gathering, patient engagement, enrolment, and monitoring process to enable direct focus on improvements and advancements that provide groundbreaking results. The possibilities for these advancements in healthcare happen only if data is gathered from many patients.
Remote data gathering is at the forefront of clinical trials advancement. It enables a smooth and timely approach to the data processor. It also enables teams to reach patients where traditional methods cannot.
We help understand and define the vision
Help define the vision
Define the product roadmap based on the value
More than 20 years of enabling clients to improve clinical research outcomes through web, mobile and related services
Our team has managed, designed and executed over 100 studies across multiple disease states.
We only employ the best. A team of organized and experienced analysts, programmers and clinical operations. Flexible to deliver your study needs
Our founding team has designed numerous applications with deep life science knowledge.
With over 100 studies across 10 solutions, we understand that each project is unique.
We work with our clients to ensure data safety & compliance across all phases of any project.
21CFR11 | GDPR | HIPAA
Let our team help you identify top identifying analytics that best fit your situation.
Over 20 years of experience across multiple solutions to help you achieve the best results.
Considering a wearable for your upcoming clinical trial? The Apple Watch is an FDA approved Class II device with a slick, beautiful and powerful utility to
Mobile technologies are gaining greater acceptance and adoption in clinical trials, to engage patients, investigators and study team 90% of SMS are opened within 3
eConsent is not just an electronic signature, it is a better way to improve clinical trial startup, reduce cost, and gain better patients. eConsent is gaining
We can help you save money, increase productivity, provide seamless collaboration and help you save lives.