Innovate Pharma Clinical Trials

Design and simulate new kinds of trials with minimal risk. Experiment with opportunities in technology, logistics, patient centricity, and real-world data. 

The Opportunity

Everyone knows that the pharma clinical trial process is expensive, time-consuming and problematic. 

How does pharma make the leap to innovative trial experiences while mitigating as many risks as possible?

Evidence-based medicine dictates treatment and payment decisions across healthcare. Scientific studies, like the randomized controlled trial, creates that evidence.
 
But the RCT, and other techniques like it, are management nightmares. They're so expensive few get done. A 2006 Institute of Medicine Round Table Report estimates that 50% to 80% of medical treatments conducted in US hospitals have insufficient evidence.
 
What if we made it easy for any medical professional to run experiments? What if we eliminated the cost and complexity?

Make the leap to innovative trial experiences while mitigating risk.

Without the need for expensive and time consuming IT investments

about ProofPilot

Speed Innovation

Build credibility. Create leadership. Bring innovations to market. Scale what works, improve what doesn't. Quickly launch anything from a tracking study to a full scale randomized controlled trial within current resources. 

healtchare research

Show Return on Investment

Evaluate programs that produce better health outcomes while showing better financial metrics. Reduce costs, increase revenue, improve health. Launch studies that used to take government academia years to plan. Use the resulting findings to make operating decisions. 

inperson engagement

Make it Local & Personal

What works for one person or community, may not work for another. Bring evidence-based and personalized medicine together. Evaluate treatments against local cultural and environmental factors. Determine what works for your population.

Design, Simulate, Launch & Manage Pharma Clinical Trials.

Design Your Study

design a healthcare research study
ProofPilot's created a visual protocol design language. Choose from a library of predefined intervention, treatment, measurement templates and functionalities. The designer supports nearly any kind of human subjects research study.
 
ProofPilot is powerful enough for a career researcher. It brings major efficiencies to a process that used to be manual. At the same time, it is easy enough to use for a first time researcher and technology novice.

Engage Participants

participant healthcare research perspective
Launch the study without any developers or IT. It's all handled. Participants can engage on any internet connected device they have access to. They don't have to download anything
 
As tasks activate and expire in your study design, they receive SMS and text messages alerting them to a new task. As a token of appreciation, they earn rewards and insights redeemed right through their device. 
 

ProofPilot even supports in-person studies. Not every task is self-service. ProofPilot provides functionality to make in person visits seemeless and efficient. 

  • Take a Tour of the ProofPilot In-Person Service Features

Technology and consumer-focused design has created massive efficiencies in the enterprise.

ProofPilot is the first and only complete platform that brings these innovations to human subjects research. 

Once you've designed your study, as the researcher you sit back and watch the data roll in. ProofPilot even includes some basic study recruitment functionality that turns participation in a study into a social-media activity. 

ProofPilot handles all the tech issues an security. All studies are run by a third-party reviewer for human subjects ethics protections

What Pharma Can Do With ProofPilot

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Highlighted Pharma Research Study Tasks

Study tasks are the basic building blocks of ProofPilot studies. Each task represents one distinct activity in your study.  Tasks are tied together with rules and organized into arms to create a full study protocol. 

ProofPilot Pharma in the News

Five Lessons that We Haven’t Learned Yet from the Theranos Scandal

There are plenty of explanations about how this was allowed to happen. Here are the five things we should be learning from the Theranos scandal.

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How to Avoid Evidence Based Cynisism

Over the past two decades, the CDC (and other health agencies) have gone all in on “evidence-based.” But they’ve done so without developing a sufficient ecosystem to produce that evidence.

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Why “Evidence Based” Is Such a Controversial Term

In the HuffingtonPost: The CDC will avoid using “evidence-based” in budget documents. If liberals and the scientific community explain this away as “bowing to the religious right,” we risk overlooking the real issue. If fiscal conservatives let this slide, we have lost one of our…

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