Download presentation
Presentation is loading. Please wait.
Published byMelanie Carroll Modified over 6 years ago
1
A non-invasive monitoring platform that collects, stores, and analyzes mobile research data
2
Problem Data colletion in research is difficult + expensive
Existing methods are archaic: Online surveys, phone calls, web portals, paper based-studies Mobile data collection is already the industry standard in commercial market research e.g. surveymonkey, qualtrics
3
Market for Clinical Trials
72,172 ongoing trials in US alone (clinicaltrials.gov) $35,750,000,000 spent annually on trials Average per-trial cost: $500,000,000 Absorbed by tax payers + consumers Average trial duration: 8 years (Department of Health and Human Services)
4
Data Collection: Problem or Solution?
Over 50% of trials still use paper clinical report forms The rest who use web-platforms still require study participants on-site to input data How we collect and manage data directly affects the length of a clinical trial
5
Data Collection: Problem or Solution?
Large Clinical Research Organizations like Pfizer, AstraZeneca, and Bayer recently started taking advantage of mobile data collection 30% reduction in trial duration 10% overall cost savings Average savings of $50,000,000 We will deliver a competitive service to pre-IPO research organizations that make up the majority of the market and have not yet realized these savings
6
Where do these savings come from? Clinical Trial Cost Components
Administrative staff $156.96 Site Monitoring $102.96mm Clinical procedure $153.52mm Central lab $67.12mm Source Data Verification $122.56mm Data Collection + Management $20.1mm Site Retention $103.04mm *Data from Dept. Health & Human Services $800,000,000 trial
7
How do we deliver this value?
The use of electronic data capture decreases the length of trials an average of 30% and reduces overall costs by 10% At home testing Reduced Source Data Verification Reduced Site Retention & Monitoring Reduced Administrative Staff Cost
8
Solution: Passify collecting, graphing & analyzing trial data
Researchers schedule mobile studies in seconds Studies are sent to users mobile devices at scheduled intervals via push notification Ex: Chronic pain measurement M-F before, during, and after work Extend studies beyond the clinical facility & reduce trial duration + retention costs
9
How does Passify Work? 3. Their results are graphed real-time, and can be compared against treatment population or per-demographic 1. Users receive scheduled studies in form of a push notification 2. They tap the notification, verify fingerprint, and use the slider to input data
10
For an 8 year study, that’s $120,000/mo
How do we make money? CRO sales models: Avg data collection & mgmt existing price point = $11,800,000 across 72,000 studies For an 8 year study, that’s $120,000/mo It costs us less than 1 cent to send a push-notification study Per-trial fee or Per-study fee Long term contracts with CRO’s conducting multiple studies
11
Alpha launch If we can cut costs, then research organizations will try our product 2 alpha tests scheduled, beta customers contingent upon initial KPI’s + Eval. 5,000 2,500 per
12
Additional customer discovery
6 California based CRO’s Clindatrix (Irvine), BIOCOM (SoCal), PPD Development (SD), PRA INTL (SD), Global Clinics (LA), Impact Clinical Trials (LA) Q1: “What business activities does your organization prioritize?” Q2: “How do you plan to address (priority)?” Q3: How are you collecting data now?
13
Q1: What business activities does your organization prioritize?
all responded with some variant of “cutting costs/shortening length of trials” 4 mentioned Risk based monitoring & source data verification reduction All mentioned site retention costs & duration of studies
14
Q2: How do you plan to address (priority mentioned)?
5/6 responded with incorporating new technologies 4/6 mentioned outsourcing more study activities None had a concise plan for incorporating new technologies All learn about new technologies at conferences and through outreach
15
Q3: How are you collecting participant data?
4/6 use paper CRF’s in one or more studies that require on-site use 2/6 use a web platform provided by a 3rd party that requires on-site use All have incorporated wearables for bioinformatic based studies (willingness to adopt mobile technologies and monitor conditions outside controlled environment)
16
Timeline Alpha study May – June
July-August analyzing studies + feedback, improving product Recruit additional beta customers through conference attendance & outreach August – Roll out dual-platform solution for beta customers We need $250,000 to deliver a competitive solution in August and directly compete with a $11,800,000 per-study price-point
Similar presentations
© 2025 SlidePlayer.com. Inc.
All rights reserved.