Science 37 alternatives for teams that need the technology without the services wrapper
Science 37 sells a virtual site service. If you want the DCT technology without the managed services wrapper, that's where WeGuide fits. A regulatory grade platform with eCOA, eConsent, wearables, and a whitelabel participant app, your coordinators running the study, six-week deployment.
No pressure, no hard sell. A 30 minute walkthrough with a research colleague who's built platforms like yours.
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Science 37's product and commercial model were both built around a specific shape of study: pharma-sponsored DCTs where the virtual site network, mobile nurses, tele-visit coordination, community clinic partnerships, is a load-bearing part of the protocol. For studies where participants need regular in-home visits, that bundle is genuinely useful. For everything else, it's services you pay for and don't use.
The fit gap shows up in a few predictable places. Mid-market sponsors can't justify bundled services pricing for studies that don't need a nurse network. Academic research teams want to configure the platform themselves rather than route every change through a services-led programme team. Registries, employee wellbeing, population health, and citizen science all sit outside Science 37's DCT-only scope. And since the eMed acquisition in 2024, some sponsors have reported uncertainty about where the Science 37 roadmap is heading.
WeGuide was built for the teams that want DCT architecture (eCOA, eConsent, whitelabel app, telehealth, wearables, remote monitoring) as a configurable platform rather than a services engagement. You keep the decentralised trial design and lose the mobile-nurse dependency, with broader use case coverage on the same system if your research portfolio includes registries, population health, or engagement programmes.
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For teams that need DCT architecture without a services wrapper, here's what changes when you move to WeGuide.
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Whitelabel participant mobile apps
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Native wearable integration
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No-code programme builder
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Here's the shortlist of platforms most teams evaluate when they're looking at alternatives to Science 37.
WeGuide
Medable
IQVIA Patient Engagement Suite
Thread Research
ObvioHealth
Curebase
Clario
All-in-one platform
WeGuide combines eCOA, eConsent, data collection, and telehealth in a single platform with whitelabel apps under your own brand.
eConsent
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Screening
Data collection
Telehealth
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Continuous engagement, not once-off surveys
Push notifications, educational content delivery, gamification, and a study companion that guides participants through the protocol. This is the difference between collecting data when a participant remembers and collecting data on schedule because the app is genuinely useful to them. The BRACE Trial achieved 90% adherence across 6,000 participants in five countries using this architecture. See WeGuide’s patient education module →
Push notifications and reminders
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Study companion
Educational content and gamification
Mobile multimodal collection
Capture the full picture of a participant's experience through forms, video, pathology, and passive sensor data all in the same app.
Forms
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Video
Pathology
Sensors
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Whitelabel: your study, your brand
WeGuide ships native iOS and Android apps fully branded under your organisation's name and identity. The app becomes the study's home for the participant, which is a big part of why our studies average 94% adherence.
Your brand end-to-end
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App store distribution
Multilingual out of the box.
Where WeGuide goes further
For teams that need the clinical layer without the rest of the Vault platform, here's what changes when you move from Veeva Clinical to WeGuide.
Technology-first, without the services wrapper
Global deployment without a mobile-nurse dependency
Broader use cases beyond DCTs
Whitelabel mobile apps under your brand
Deploy in weeks with a no-code programme builder
Native wearable integration
Independent roadmap
Australian data residency and TGA certification
Built for regulated research
Every WeGuide study runs on our managed infrastructure. Your IT team doesn't patch servers, manage backups, or run disaster recovery drills.
TGA Certified
ISO 27001
Data Hosted in Australia
GDPR Compliant
Biometric Security
256-bit AES Encryption
Faster
Your own platform ready in weeks and changes are made in minutes
Adherence Rates
High patient engagement and better quality data
Cost Saving
Reduce financial and technology risk when creating a secure health app
Patients Impacted
With our ease of use and roll out, our apps have engaged 200k+ users
Where Science 37 excels
Science 37 has a genuine place in the DCT market, and an honest comparison has to start with what the platform does that no one else does.
The Metasite virtual site network. This is the differentiator. Science 37 runs a network of mobile nurses, community clinics, and tele-visit infrastructure that sponsors can book as a managed service. For a DCT where participants need regular in-home visits, physical sample collection, or local clinic access in geographies where the sponsor doesn't have a site footprint, this is a capability no pure technology platform offers. If your protocol depends on it, Science 37's the right choice.
DCT pioneer with sponsor relationships. Science 37 has been running decentralised trials with pharma sponsors since well before DCT was a category name. That track record, plus the Phase II and III experience, creates real institutional trust with sponsor therapeutic area teams who've already worked with the platform.
End-to-end delivery. For sponsors who want a single vendor handling the technology, the virtual site operations, and the patient logistics as one programme, Science 37's integrated model removes a coordination layer. That's a genuine operational benefit if your internal team doesn't have the capacity to manage multiple vendors.
Public-company history and industry recognition. Science 37 has been named in analyst reports, peer-reviewed publications, and industry rankings across multiple years. For sponsors whose procurement or governance processes weigh analyst coverage, that history carries weight.
If your study needs the Metasite network, and the services wrapper is what makes the trial possible rather than an extra cost, Science 37 is the defensible choice. We'd rather say that honestly than oversell what WeGuide does.
WeGuide works alongside your existing site network
If your study needs occasional in-person visits but doesn't need a full Metasite virtual site network, WeGuide runs the digital layer (eCOA, eConsent, engagement, wearables, telehealth) while your existing investigator sites or a partner nursing service handles the physical touchpoints. Our Integration Engine connects through APIs, so visit schedules, sample tracking, and participant status stay in sync across systems. Teams typically combine this with their existing EDC and site coordination tools.
How the switch works
For teams moving from Science 37 to WeGuide, or running WeGuide alongside Science 37 for studies that don't need the Metasite network, here's how onboarding typically plays out.
Discovery Call
A 30-minute conversation with one of our research delivery team. We look at your protocol, your current Science 37 setup, and which parts of the services wrapper you actually need. No sales pitch.
Study Configuration
Our team works alongside yours to configure the study in WeGuide. Typical timeline: two to four weeks. Mid-study migrations from Science 37 typically plan for around six weeks of transition, with data export via the Integration Engine.
Participant Onboarding
The whitelabel app goes live. Your research coordinators invite participants, who download the app under your organisation's brand. eCOA instruments, consent flows, and engagement templates are ready.
Ongoing Support
You get a named research delivery contact, not a ticketing queue. We stay involved for the life of the study.
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BRACE Trial (Murdoch Children's Research Institute)
A global randomised controlled trial studying whether the BCG vaccine could reduce COVID-19 symptom severity. Launched across five countries with 6,000+ participants in six weeks during the pandemic. Adherence exceeded 90%. The study needed decentralised architecture and global reach, without a Metasite-style virtual site network, and WeGuide delivered the digital layer while investigator sites handled in-person visits.
GenV (Generation Victoria)
A population health study tracking more than 100,000 Victorian families from birth. Longitudinal registry work at this scale sits outside Science 37's DCT focused scope. The whitelabel family facing app is the reason retention has held across multiple years.
Lendlease wellbeing programme
An employee wellbeing deployment across a global workforce, using WeGuide's platform for participant reported outcomes, engagement content, and population health analytics. Completely outside DCT software scope, and the kind of programme that shows what a broader patient engagement platform enables.
Questions
Straight answers on how WeGuide compares to Science 37, what migration looks like, and when staying on Science 37 is the right call.
Is WeGuide a full replacement for Science 37?
Not in every case, and we'll tell you that honestly. Science 37's Metasite virtual site network, with mobile nurses, community clinics, and tele-visit infrastructure delivered as a managed service, is genuinely unique and valuable for trials that need physical presence at participants' homes or in local communities. If your protocol depends on a virtual site network, Science 37 (or their successor model post-eMed) is the right choice. WeGuide is the right choice when you need DCT architecture (eCOA, eConsent, telehealth, wearables, whitelabel app, engagement) as a configurable technology platform, and your in-person visits can be handled through your existing site network or a partner nursing service.
Does WeGuide do decentralised clinical trials?
Yes. Decentralised trial architecture is a core WeGuide use case. Telehealth, eConsent, remote monitoring, eCOA, whitelabel participant apps, wearables, and engagement are all built in. The BRACE Trial is a good example of what a rapid-deploy decentralised trial looks like on our platform: 6,000+ participants across five countries in six weeks. The difference from Science 37 is that WeGuide runs the digital layer and leaves physical site operations to your existing network, rather than bundling a virtual site service alongside the software.
How does WeGuide handle in person visits that used to require a Science 37 mobile nurse?
We coordinate with the sponsor's existing site network or with partner nursing services. WeGuide doesn't operate its own nurse network. For studies that need predictable mobile nurse coverage at scale, Science 37's Metasite model or a dedicated nursing partner is a better architectural fit than WeGuide on its own.
How does pricing compare?
Science 37 typically combines the platform with virtual site services in project-based pricing, which means you're paying for both the technology and the services together. WeGuide is technology-only project pricing with every module included in the core licence. For studies that don't need the full Metasite services wrapper, WeGuide is typically lower-cost; for studies that do need the network, a direct pricing comparison is harder because you'd be comparing different scopes.
What's the status of Science 37 post-eMed acquisition?
Science 37 was acquired by eMed in 2024. The combined entity's roadmap and product continuity have shifted, and some sponsors have reported uncertainty about where the Science 37 platform is heading under the new ownership structure. WeGuide's product roadmap is independently set by our product team alongside research delivery partners, and the platform has been in continuous development as WeGuide for seven years (with 15 years of combined digital health expertise behind it).
Can we migrate from Science 37 to WeGuide mid-study?
Possible, with planning. Mid study migrations typically need around six weeks for data export via the Integration Engine, regulatory documentation alignment, and participant re onboarding into the new whitelabel app. We'd walk through the specifics of your study on a discovery call before committing to a timeline; some protocols (especially those mid enrolment in a late stage Phase III) are genuinely harder to migrate than others.
Does WeGuide support the kinds of trials Science 37 is known for?
For decentralised trials where the Metasite virtual site network is load-bearing, no. For decentralised trials where the digital layer (eCOA, eConsent, telehealth, wearables, engagement) is the critical component and in person touchpoints are handled through existing site networks, yes, and this is the most common shape of study we run.
Compare WeGuide to other clinical trial platforms
Eleven more honest platform comparisons, from academic EDC to enterprise pharma.
Veeva Vault Clinical
Life sciences cloud
Thread Research
Virtual CRO + software
Clario
eCOA specialist
Oracle Clinical
Clinical One & InForm
OpenClinica
Open-source EDC
Medable
DCT for top-50 pharma
IQVIA
Full-service CRO
Florence Healthcare
Site-side workflow
Science 37
Open-source EDC
obviohealth
Virtual site service
Medidata Rave
Enterprise pharma stack
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