Healthcare, Medical, and Software Research

Healthcare, Medical, and Software Research

Healthcare, Medical, and Software Research

End-to-End Research Support for MedTech, Life Sciences, and Digital Health

You’re building solutions that can improve lives, and proving their value takes more than a good idea. You need solid research design, regulatory approval, and the ability to translate data into actionable, publishable results. That’s where we come in.

At Estenda Solutions, we provide clinical and digital health research support to help MedTech, Life Sciences, and digital health companies design, execute, and publish impactful studies. Whether you’re developing a new medical device, testing a digital therapeutic, or validating clinical software, we help you turn evidence into innovation.

Let's Discuss Your Research Project

Let's Discuss Your Research Project

Let's Discuss Your Research Project

Why Choose Estenda for Medical and Digital Health Research?


You're not just running a study, you’re advancing science, improving care, and aiming for real-world impact. Estenda has over 20 years of experience supporting Life Sciences research, clinical research, and medical software validation, from idea to IRB to publication.


What sets us apart:


  • Successful partnerships with NIH, Robert Wood Johnson Foundation, and other major funders.

  • Deep experience in grant writing for medical research and submission strategy.

  • Proven support for study design, IRB compliance, and real-world evidence (RWE) generation.

  • Advanced data analytics in medical research using AI, machine learning, and predictive modeling.

  • Strong track record of peer-reviewed journal publications and conference presentations.

Our Clinical, Medical, and Digital Health Research Services

Our research team collaborates with you to design, execute, and analyze studies that drive real-world improvements in digital health, medical technology, and clinical decision-making to help you generate evidence, meet regulatory standards, and share your breakthroughs with the world.

Grant Writing & Research Funding Support

Design Research That Proves Value and Drives Adoption

We help you develop research protocols that stand up to scientific scrutiny and regulatory standards — whether you're conducting clinical validation for software, testing a digital therapeutic, or running a device trial.


  • Study Design for Clinical and Digital Health Research

  • Pilot Studies & Feasibility Assessments

  • Methodology Frameworks for MedTech Validation

Study & Protocol Design

IRB Strategy & Regulatory Compliance

Data Analytics & Research Insights

Clinical & Digital Health Outcomes Reporting

Journal Publications & Conference Presentations

Grant Writing & Research Funding Support

Design Research That Proves Value and Drives Adoption

We help you develop research protocols that stand up to scientific scrutiny and regulatory standards — whether you're conducting clinical validation for software, testing a digital therapeutic, or running a device trial.


  • Study Design for Clinical and Digital Health Research

  • Pilot Studies & Feasibility Assessments

  • Methodology Frameworks for MedTech Validation

Study & Protocol Design

IRB Strategy & Regulatory Compliance

Data Analytics & Research Insights

Clinical & Digital Health Outcomes Reporting

Journal Publications & Conference Presentations

Grant Writing & Research Funding Support

Design Research That Proves Value and Drives Adoption

We help you develop research protocols that stand up to scientific scrutiny and regulatory standards — whether you're conducting clinical validation for software, testing a digital therapeutic, or running a device trial.


  • Study Design for Clinical and Digital Health Research

  • Pilot Studies & Feasibility Assessments

  • Methodology Frameworks for MedTech Validation

Study & Protocol Design

IRB Strategy & Regulatory Compliance

Data Analytics & Research Insights

Clinical & Digital Health Outcomes Reporting

Journal Publications & Conference Presentations

Related Case Studies

Real Results from Real AI in MedTech & Life Sciences

We’ve helped MedTech companies improve diagnostics, reduce R&D timelines, and scale faster with custom AI and machine learning solutions. Check out how we’ve delivered results—without compromising compliance or quality.

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Project HealthDesign: Pioneering Next-Generation Personal Health Records

Robert Wood Johnson Foundation

Project HealthDesign: Pioneering Next-Generation Personal Health Records

Robert Wood Johnson Foundation

Project HealthDesign: Pioneering Next-Generation Personal Health Records

Robert Wood Johnson Foundation

Community-Driven Research – A Platform for Engaging the Public in Health Research

Patient-Centered Outcomes Research Institute (PCORI)

Community-Driven Research – A Platform for Engaging the Public in Health Research

Patient-Centered Outcomes Research Institute (PCORI)

Community-Driven Research – A Platform for Engaging the Public in Health Research

Patient-Centered Outcomes Research Institute (PCORI)

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From Our Experts

Explore expert articles and blogs covering industry trends, best practices, and innovative applications of AI/ML in healthcare.

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research and development

Why Is Choosing the Right Research and Development Partner Crucial for MedTech Companies?

research and development

Why Is Choosing the Right Research and Development Partner Crucial for MedTech Companies?

research and development

Why Is Choosing the Right Research and Development Partner Crucial for MedTech Companies?

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Frequently Asked Questions

What types of research does Estenda support?

We support clinical, digital health, software validation, and data-driven research in areas such as telehealth, patient outcomes, AI-driven healthcare, and population health analytics. Our expertise includes protocol design, IRB approvals, data analytics, and regulatory compliance.

Can you help secure research funding and write grant proposals?

Yes, we have successfully secured funding from NIH, the Robert Wood Johnson Foundation, and other major organizations. Our team provides grant writing, submission strategy, and budget planning support to maximize funding opportunities.

How can you help us validate our medical device or digital health product through clinical research?

We work with you to design IRB-approved studies that generate clinical and real-world evidence. From protocol development to data collection and analytics, we help ensure your study supports product claims, regulatory submissions, and market acceptance.

We need to generate real-world evidence (RWE) for FDA or payers — can Estenda support that?

Absolutely. We help you design and execute RWE studies that demonstrate product safety, effectiveness, and health economics. Our team supports data collection, outcome measurement, and reporting aligned with payer and regulatory requirements.

Can you support software validation research for SaMD or clinical decision support tools?

Definitely. We help design validation studies for software as a medical device (SaMD) and CDS tools, supporting FDA guidance, clinical testing protocols, and AI performance measurement in real-world settings.

How do I start a research project with Estenda?

Start with a quick strategy call. We’ll discuss your goals, data challenges, funding opportunities, and what success looks like. From there, we help you build a plan, from protocol to publication, that’s tailored to your mission.

What types of research does Estenda support?

We support clinical, digital health, software validation, and data-driven research in areas such as telehealth, patient outcomes, AI-driven healthcare, and population health analytics. Our expertise includes protocol design, IRB approvals, data analytics, and regulatory compliance.

Can you help secure research funding and write grant proposals?

Yes, we have successfully secured funding from NIH, the Robert Wood Johnson Foundation, and other major organizations. Our team provides grant writing, submission strategy, and budget planning support to maximize funding opportunities.

How can you help us validate our medical device or digital health product through clinical research?

We work with you to design IRB-approved studies that generate clinical and real-world evidence. From protocol development to data collection and analytics, we help ensure your study supports product claims, regulatory submissions, and market acceptance.

We need to generate real-world evidence (RWE) for FDA or payers — can Estenda support that?

Absolutely. We help you design and execute RWE studies that demonstrate product safety, effectiveness, and health economics. Our team supports data collection, outcome measurement, and reporting aligned with payer and regulatory requirements.

Can you support software validation research for SaMD or clinical decision support tools?

Definitely. We help design validation studies for software as a medical device (SaMD) and CDS tools, supporting FDA guidance, clinical testing protocols, and AI performance measurement in real-world settings.

How do I start a research project with Estenda?

Start with a quick strategy call. We’ll discuss your goals, data challenges, funding opportunities, and what success looks like. From there, we help you build a plan, from protocol to publication, that’s tailored to your mission.

What types of research does Estenda support?

We support clinical, digital health, software validation, and data-driven research in areas such as telehealth, patient outcomes, AI-driven healthcare, and population health analytics. Our expertise includes protocol design, IRB approvals, data analytics, and regulatory compliance.

Can you help secure research funding and write grant proposals?

Yes, we have successfully secured funding from NIH, the Robert Wood Johnson Foundation, and other major organizations. Our team provides grant writing, submission strategy, and budget planning support to maximize funding opportunities.

How can you help us validate our medical device or digital health product through clinical research?

We work with you to design IRB-approved studies that generate clinical and real-world evidence. From protocol development to data collection and analytics, we help ensure your study supports product claims, regulatory submissions, and market acceptance.

We need to generate real-world evidence (RWE) for FDA or payers — can Estenda support that?

Absolutely. We help you design and execute RWE studies that demonstrate product safety, effectiveness, and health economics. Our team supports data collection, outcome measurement, and reporting aligned with payer and regulatory requirements.

Can you support software validation research for SaMD or clinical decision support tools?

Definitely. We help design validation studies for software as a medical device (SaMD) and CDS tools, supporting FDA guidance, clinical testing protocols, and AI performance measurement in real-world settings.

How do I start a research project with Estenda?

Start with a quick strategy call. We’ll discuss your goals, data challenges, funding opportunities, and what success looks like. From there, we help you build a plan, from protocol to publication, that’s tailored to your mission.