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.

patient engagement

Used by leading research and medical institutes.

Why research teams look for a Science 37 alternative

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.

Full comparison: WeGuide vs Science 37
Functionality
Primary use case
Patient engagement platform with eCOA, eConsent, registries, telehealth
Academic survey and data collection
Primary use case
Patient engagement platform with eCOA, eConsent, wearables, registries
Clinical layer of the broader Vault life sciences cloud
Primary use case
Patient engagement platform with integrated eCOA, eConsent, wearables, registries, and wellbeing
DCT platform with eCOA, eConsent, EDC, telehealth, plus outcome measure and patient voice consulting
Primary use case
Patient engagement and clinical trial platform for mid-market sponsors, academic research, registries, DCTs
Decentralised trial delivery with virtual site services for pharma sponsors
Participant mobile app
Whitelabel iOS and Android under your brand
Mobile browser view, REDCap-branded
Business model
Pure technology
Platform plus consulting (Modus, inVibe)
Model
Technology platform only
Platform plus virtual site services
Hosting model
Managed cloud (ISO 27001, HIPAA, GDPR, 21 CFR Part 11, TGA Class I)
Self-hosted by each institution on its own servers
Target customer
Mid-market sponsors, academic CROs, digital health programmes, registries
Enterprise pharma running Vault across commercial, regulatory, quality, and clinical
Business model
Pure technology platform, no consulting scope
Platform plus consulting services (Modus Outcomes, inVibe)
Target customer
Mid-market sponsors, academic research, CROs, registries, digital health programmes
Pharma sponsors running DCTs with in home or community clinic visits
Commercial model
Managed SaaS, project-based pricing
Free, self-hosted (institutional IT required)
Whitelabel app
Yes
Thread-branded Study Companion and PatientFirst eCOA
Virtual site network
Not offered (partners with existing sites)
Proprietary Metasite mobile nurse network
Whitelabel mobile app
Yes, fully branded under your organisation
No, web view only
Configuration model
No-code programme builder, self-service by research teams
Dedicated Vault administrators, enterprise implementation projects
Target customer
Mid-market sponsors, academic research, CROs, registries, health organisations
Pharma sponsors, biotech, CROs running DCTs and hybrid trials
Delivery model
Technology platform you configure directly
Technology plus managed virtual site services (Metasite)
Wearable integration
Native Garmin, Apple Health, Google Fit
Not offered
Native EDC
Integrates with external EDCs
Native Thread EDC
Whitelabel app
Yes
Science 37-branded
eCOA and ePRO
Native with 200+ validated instrument library
Custom surveys, no validated instrument library
Typical deployment time
6 weeks (BRACE Trial: 6,000 participants across 5 countries)
Enterprise implementation cycles, typically multi-month
Device model
BYOD-first (participants' own phones)
BYOD-first with sensor and wearable integrations
Typical deployment time
6 weeks (BRACE Trial: 6,000 participants across 5 countries)
Project based, services led engagement cycles
eConsent with version control
Built in
Bolt-on, limited capability
Outcome measure consulting
Not offered
Modus Outcomes (acquired)
No-code programme builder
Yes
Services-led configuration
eConsent
Built-in with regulatory version control
Not available natively
Pricing model
Project-based, all modules included
Enterprise annual contracts, typically tied to broader Vault commitments
Whitelabel mobile app
Yes, fully branded under your organisation
Thread-branded Study Companion and PatientFirst eCOA
Pricing model
Project based, all modules included, scales to study complexity
Project based with services components bundled
200+ validated instrument library
Yes, integrated into Form Builder
Survey library exists, not validated instrument-first
Patient voice qualitative analytics
Not offered
inVibe (acquired)
Roadmap stability
Independent product roadmap
Post-eMed-acquisition shifts (2024)
Wearable integration
Native Garmin, Apple Health, Google Fit
Not available natively
Whitelabel mobile app
Yes, fully branded under your organisation
MyVeeva for Patients carries Veeva branding
eCOA instrument library
200+ validated instruments integrated into Form Builder
PatientFirst eCOA with global instrument library
eCOA and ePRO
Native with 200+ validated instrument library
eCOA and ePRO included in the DCT stack
Longitudinal engagement
Automated reminders, in-app messaging, push notifications, study companion
Email invitations, manual follow-up
eCOA and ePRO
Native with 200+ validated instrument library
MyVeeva for Patients covers eCOA and ePRO
eConsent
Built-in with regulatory version control and re-consent workflows
Integrated in platform
eConsent
Built-in with regulatory version control
Built-in with regulatory version control
Multi-language
Built-in translation management (proven on INHERIT study)
Manual translation per form
Telehealth
Built-in video visits and virtual site features
Virtual Visits as a core feature
Whitelabel mobile app
Yes, fully branded under your organisation
Science 37 branded participant experience
No-code programme builder
Yes, research teams configure studies directly
Form-level yes, but engagement and app experience require external tools
Wearable integration
Native Garmin, Apple Health, Google Fit
Supported through partner integrations
EDC
Integrates with external EDCs (Rave, Vault, REDCap, Viedoc, Clinion)
Native Thread EDC
Virtual site network (mobile nurses, community clinics)
Not offered; we coordinate with sponsor site networks
Metasite network (unique in market)
REDCap integration
Two-way sync via Integration Engine, pick up where REDCap leaves off
Native platform
Telehealth and virtual visits
Built-in video visit and virtual site features
MyVeeva for Patients covers virtual visits
Wearable integration
Native Garmin, Apple Health, Google Fit
Sensor and wearable integrations
Native wearable integration
Native Garmin, Apple Health, Google Fit
Supported through partner integrations
deployment-time
Typical 6 weeks for a full study launch
Depends on institutional IT; days for simple forms, months for custom builds
Patient registry
Built-in longitudinal registry (GenV: 100,000+ families)
Not a native use case
Patient registry
Built-in longitudinal registry capability (FSHD Global Registry)
Not a native offering
Telehealth
Built-in video visit and virtual site features
Built-in tele-visit capabilities
Regulatory certification
TGA certified Class I medical device software
Depends on each institution's hosting configuration
Employee wellbeing and population health
Built-in (Lendlease programme)
Outside the platform's scope
Employee wellbeing and population health
Built-in (Lendlease, GenV)
Not a primary use case
Patient registry
Built-in longitudinal registry (GenV: 100,000+ families)
Not a native use case
Pricing
Project-based, includes hosting, support, and all modules
Free licence, but institutional IT, server hosting, maintenance, and developer time not included
EDC
Form Builder covers eCRF use cases, deeper capture via Integration Engine
Vault EDC, a direct Medidata Rave competitor with strong Vault-customer adoption
Citizen science and multilingual community studies
Built-in (INHERIT)
Not a primary use case
Employee wellbeing and population health
Built-in (Lendlease programme)
Outside the platform's scope
Life sciences cloud breadth
Clinical and participant layer only
Full Vault platform: CRM, QMS, RIM, PromoMats, Clinical
Multi-language translation management
Built-in (INHERIT study proof)
Available in enterprise Vault
Outcome measure consulting
Not offered (technology only)
Modus Outcomes (acquired)
No-code programme builder
Yes, research teams configure studies directly
Services-led configuration
Regulatory certification
TGA Class I medical device, ISO 27001, 21 CFR Part 11, HIPAA, GDPR
21 CFR Part 11 and broad regulatory compliance across Vault
Patient voice qualitative analytics
Not offered
inVibe (acquired)
Regulatory certification
TGA Class I medical device, ISO 27001, 21 CFR Part 11, HIPAA, GDPR
21 CFR Part 11, DCT regulatory track record
Australian data residency
Yes
Regional options via Veeva global infrastructure
No-code programme builder
Yes, research teams configure studies directly
PatientFirst eCOA is no-code; broader configuration is services-led
Australian data residency
Yes
Not native
Regulatory certifications
TGA Class I, ISO 27001, 21 CFR Part 11, HIPAA, GDPR
21 CFR Part 11, HIPAA, GDPR
Ownership continuity
Independently roadmapped
Acquired by eMed in 2024
Australian data residency
Yes
Not a primary offering
Pricing model
Project-based, all modules included, technology only
Enterprise project-based, often includes consulting scope
Deployment time
Typical 6 weeks
Study-dependent, services-led timelines
Top alternatives to Science 37 in 2026
Here's the shortlist of platforms most teams evaluate when they're looking at alternatives to Science 37.
Alternative #1
WeGuide
A patient engagement and clinical trial platform covering eCOA, eConsent, telehealth, wearables, registries, and analytics in a single system with whitelabel mobile apps under your own brand. TGA certified Class I, ISO 27001, 21 CFR Part 11, HIPAA and GDPR compliant. Designed for mid-market sponsors, academic research, CROs, and digital health programmes that need DCT architecture without a services wrapper.
Best For
mid-market DCTs, patient registries, decentralised observational studies, academic research, CRO work, digital health programmes.
Alternative #2
Medable
One of the most established DCT platforms, with deep pharma sponsor relationships, a comprehensive eCOA and eConsent suite, and a long FDA submission track record. Typically a fit for top-50 pharma sponsors running late-stage decentralised trials with enterprise implementation budgets.
Best For
top-50 pharma sponsors running enterprise DCTs with FDA-facing submissions.
Alternative #3
IQVIA Patient Engagement Suite
IQVIA's decentralised trial and patient engagement technology, usually bundled with IQVIA's CRO services, real-world data offerings, and site network. Enterprise positioning with the IQVIA brand and operational footprint behind it, similar to Science 37's services-heavy model but at a larger scale.
Best For
enterprise sponsors who want DCT technology bundled with IQVIA CRO services.
Alternative #4
Thread Research
A DCT platform with strong eCOA, telehealth, and ePRO capabilities, acquired into Reify Health in 2023. The Modus Outcomes and inVibe acquisitions added patient centred outcome measure consulting and qualitative patient voice analytics.
Best For
mid-market sponsors who want lighter weight DCT technology with eCOA consulting services alongside.
Alternative #5
ObvioHealth
A virtual clinical trial platform with its own ObvioGo app, focused on eCOA, ePRO, and virtual site management. Popular with consumer health and nutraceutical sponsors who want a fast, participant-centric digital study experience.
Best For
consumer health, nutraceutical, and virtual observational studies.
Alternative #6
Curebase
A decentralised trial platform focused on running hybrid and fully virtual studies with a patient-first design philosophy. Popular with biotech and mid-market sponsors who want a modern DCT tool without enterprise overhead.
Best For
biotech and mid-market sponsors running hybrid and virtual trials.
Alternative #7
Clario
The deepest eCOA specialist in the market (formed from the ERT and Bioclinica merger). Strongest in cardiac safety, medical imaging, respiratory, and precision motion endpoints. Not a general-purpose DCT platform, but a must-consider if your study needs specialised endpoint capture.
Best For
pharma trials requiring specialised eCOA endpoints (cardiac, imaging, respiratory).

All-in-one platform

WeGuide combines eCOA, eConsent, data collection, and telehealth in a single platform with whitelabel apps under your own brand.

eConsent

Regulatory grade electronic consent with version tracking, re-consent workflows, digital signatures, and audit trails. REDCap doesn't have native eConsent, so teams either pair it with a second vendor or manage consent on paper.
We Guide

Screening

Screen participants against eligibility criteria directly in the app before they enrol, with branching logic and automated routing to the right study arm.

Data collection

Native eCOA and ePRO with a 200+ validated instrument library, custom forms with branching logic, and multimodal capture through forms, video, active tasks, and sensors.

Telehealth

Built in video visits, asynchronous messaging, and remote assessments that keep participants engaged with their research team between site visits.

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

Scheduled push notifications, smart reminders, and re engagement flows that meet participants where they are on their phone rather than waiting for them to check an email.
We Guide

Study companion

A dedicated study companion that explains what's coming next, why it matters, and how to complete it ensuring participants stay informed and on track throughout the entire journey.

Educational content and gamification

Contextual educational content, progress tracking, and gentle gamification that keep participants engaged across multi year longitudinal studies.

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

Native eCOA and ePRO instruments with branching logic, validation, and offline support. 200+ validated instruments ready to drop into a study.
We Guide

Video

Structured video capture for symptom diaries, gait analysis, and remote clinical assessments, stored securely against the participant record.

Pathology

Seamlessly set up integrations with your pathology providers to collect DNA or blood data from participants, streamlining the clinical data pipeline directly within the study workflow.

Sensors

Native Garmin, Apple Health, Google Fit, and FindAir integrations that sync passive wearable and sensor data straight into the study database.

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

Native iOS and Android apps under your organisation's name, logo, and colours not a WeGuide-branded web view.
We Guide

App store distribution

Published under your developer account on the Apple App Store and Google Play so participants download an app that clearly belongs to your institution.

Multilingual out of the box.

Translation management for multisite, multi-country studies, proven on INHERIT across multilingual communities.

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

Certified Class I medical device software under the Therapeutic Goods Administration.

ISO 27001

Certified information security management covering access, audit, and incident response.

Data Hosted in Australia

Participant data is hosted in Australian data centres with sovereign data controls.

GDPR Compliant

GDPR, HIPAA, and 21 CFR Part 11 ready for multi-country and US-based studies.

Biometric Security

Participant access protected by PIN code and biometric authentication on device.

256-bit AES Encryption

All data encrypted at rest and in transit with automated backups and disaster recovery.
12x

Faster

Your own platform ready in weeks and changes are made in minutes

94%

Adherence Rates

High patient engagement and better quality data

10x

Cost Saving

Reduce financial and technology risk when creating a secure health app

200K+

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.

We Guide

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.

Case studies: research teams running DCTs without a services wrapper
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.

Helping researchers transform ideas into discoveries.

Hear what our clients have to say!

"GenV trusted WeGuide to run a multi-year population health study across more than 100,000 Victorian families. Longitudinal engagement at this scale requires push notifications, multi-modal data capture, and a whitelabel app that families will keep on their phones for years.""
Susan Clifford
Susan Clifford
Senior Research Officer
GEN V logo
“The main benefit of WeGuide is its convenience. I can’t imagine how we would follow thousands of participants and collect their data without WeGuide!”
Kaya Gardiner
Kaya Gardiner
Trial Project Manager
Murdoch children Research Institute
"WeGuide has transformed how we manage our patient registry. The ease of digital screening and obtaining eConsent has significantly improved our workflow."
Emma Photo
Emma Weatherley
Managing Director
FSHD Global
"The WeGuide trial offers staff a practical tool for recording daily COVID-19 symptoms and temperatures. For those in high-risk areas, daily reminders and alerts provide peace of mind and reassurance about their health."
KATE Cranwell
Kate Cranwell
Manager
Western Health
"It’s obvious that WeGuide is committed to develop technology that benefits people in the community. WeGuide has been a great partner in achieving this goal within Western Health."
Testimonial Photo
Paul Eleftheriou
Chief Medical Officer
Western Health

Questions

Straight answers on how WeGuide compares to Science 37, what migration looks like, and when staying on Science 37 is the right call.

Contact us

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

Never miss an update

Get all the latest news, blog posts and product updates from WeGuide, delivered directly to your inbox. We'll rarely send more than one email a month.

By clicking Organise a demo, you're confirming that we can contact you to set up a demonstration.

Thank you! Your submission has been received!
Oops! Something went wrong. Please try again.

Certified and Compliant by Leading Standards