Developer docs
API playgroundTry for free, no card

Search company profiles

Clario

Full company profile

uuid0009w88

Namestring
Clario
Legal namestring
Clario
Websiteurl
clario.com
Company typeenum
Private
Founded yearint
2021
Descriptiontext

Clario is a clinical trial endpoint technology company that provides data and technology solutions for drug and medical device approvals across pharmaceutical, biotechnology, and Contract Research Organization (CRO) customers. Formed in 2021 through the merger of ERT (eResearchTechnology) and Bioclinica, the company operates a cloud-native integrated platform spanning six core product lines: Cardiac Solutions (ECG, arrhythmia, blood pressure, Phase I/TQT assessment); eCOA (electronic clinical outcome assessments including neuroscience, oncology, rater training, and the eC-SSRS for suicidal ideation monitoring); Medical Imaging (centralized core lab with AI-powered redaction and SMART Submit); Precision Motion (Opal V2R/V2C wearable sensors for digital mobility endpoints); Respiratory Solutions (SpiroSphere, home spirometry, oscillometry); and Clinical Adjudication (centralized endpoint committee platform with 15,000+ active users across 61 countries). The platform is supported by Trial Enablement software and AI Solutions with 120+ proprietary AI models deployed across 600+ active trials. Notable proprietary technologies include the FDA-cleared SpiroSphere with wireless ECG, the EPQT (Early Precision QT) methodology enabling potential TQT waiver qualification, and Opal sensors capable of predicting fall risk in Parkinson's patients with 84-92% accuracy.

Clario's go-to-market is enterprise field sales targeting pharmaceutical sponsors, biotech companies, and CROs globally, with study-by-study pricing that scales with therapeutic area, endpoints, geographies, languages, patient volume, and study duration. Sales cycles are long and technically complex, requiring deep scientific and regulatory expertise. The company has supported over 30,000 clinical trials across more than 100 countries with translations in over 100 languages, contributing to approximately 70% of FDA and EMA novel drug approvals since 2015 (700+ approvals). It maintains 70,000+ active trial sites, ships 136,000 validated devices per year through logistics hubs in the US, EU, and Japan, and has engaged 2.8 million+ patients through its eCOA Rapid Start catalog and 500,000+ patients in eCOA neuroscience trials.

Revenue derives primarily from clinical trial endpoint services billed study-by-study under multi-year enterprise agreements, supplemented by technology licensing and platform access. 2025 revenue was projected at approximately $1.25 billion prior to Clario's acquisition by Thermo Fisher Scientific, completed in March 2026 for $8.875 billion in cash plus up to $525 million in earnout payments — representing an exit for private equity sponsors Astorg, Cinven, Nordic Capital, and Novo Holdings. Post-acquisition, Clario operates as a subsidiary within Thermo Fisher's clinical research services segment.

Short descriptiontext

Clario is a clinical trial endpoint technology company providing cloud-native eCOA, cardiac safety, medical imaging, precision motion, and respiratory solutions to pharmaceutical, biotech, and CRO sponsors across 100+ countries, supporting 70% of FDA/EMA novel drug approvals since 2015.

Operating statusenum
Acquired
Ownership categoryenum
Headcount rangeband
1,001–5,000
akta.pro rankint
HeadquartersPhiladelphia, United States
HQ citystring
Philadelphia
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices3 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
clinical trial endpoints, cardiac safety monitoring, electronic clinical outcomes, medical imaging core lab, clinical trial technology
Industry3 codes
1Clinical Trial Informatics (EDC/CTMS/eCOA/eTMF)
CodeHLAGAJAMPrimaryYes
2Clinical CROs (Phase I–IV)
CodeHLAGAAAAPrimaryNo
3Clinical Data Management, Biostatistics & Statistical Programming CROs
CodeHLAGAAAFPrimaryNo
NAICS code3 codes
  • Computer Systems Design and Related Services54151
  • Medical and Diagnostic Laboratories6215
  • Analytical Laboratory Instrument Manufacturing334516
SIC code3 codes
  • Services-Prepackaged Software7372
  • Services-Medical Laboratories8071
  • Surgical & Medical Instruments & Apparatus3841
Product category
Clinical Trial Endpoint Technology
Social media profiles2 records
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model2 records
1Clinical Trial Endpoint Solutions
TypeSubscription Recurring
Description

Clario generates revenue by providing endpoint data solutions to pharmaceutical and biotech companies conducting clinical trials. Services are priced study-by-study based on complexity, scope, geographic reach, and duration. Revenue projected at approximately $1.25 billion in 2025 prior to acquisition by Thermo Fisher.

clario.com
2Technology Licensing and Platform Access
TypeLicensing Royalties
Description

Revenue from licensing proprietary technology platforms, AI models, and specialized assessment tools to clinical trial sponsors and CROs.

ehealth.eletsonline.com
Marketing channels7 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components5 values
Personnel, Technology or R&D, Operations, Infrastructure, Marketing or Sales
Pricing details1 tier
1Enterprise study-based pricing
ModelSubscriptionBilling cadenceMulti-year contract
Notes

Quote-based pricing tailored to individual study requirements. Factors include therapeutic area, endpoints required, countries, languages, patient volume, and study phase.

clario.com
GTM typeB2B
B2B
Offering typeSoftware
Software
Brand1 of 10 records shown
1eResearchTechnology (ERT)
Description

Legacy brand for cardiac safety solutions, part of Clario's portfolio

clario.com
+9 more records
Core offering1 text field

Clario provides technology-enabled endpoint data solutions for clinical trials that collect, process, and analyze data used to support drug and medical device approvals. Its offerings span six core endpoint categories: Cardiac Solutions (centralized ECG, arrhythmia analysis, blood pressure, Phase I/TQT assessment), eCOA (electronic patient-, clinician-, and performance-reported outcomes including neuroscience modules), Medical Imaging (centralized imaging core lab with SMART Submit platform), Precision Motion (Opal® wearable sensors for mobility endpoints), Respiratory Solutions (spirometry, oscillometry, SpiroSphere® device), and Clinical Adjudication (centralized endpoint committee platform). Supporting capabilities include Trial Enablement software, Hybrid Trials services, and an AI platform with 120+ models, all delivered globally across 100+ countries.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 7 values shown
  • 70% of FDA and EMA novel drug approvals since 2015 supported by Clario's platform
+6 more records
Product overview1 text field

Clario is a clinical trial endpoint technology company offering a comprehensive platform of endpoint solutions for clinical trials. The portfolio includes six core products: Cardiac Solutions (ECG, arrhythmia, blood pressure monitoring with regulatory consulting), eCOA (electronic clinical outcome assessments including neuroscience, oncology, and specialized modules like Swift, Rapid Start, and training), Medical Imaging (centralized core lab services with SMART technology), Precision Motion (Opal® wearable sensors for mobility), Respiratory Solutions (spirometry, home testing, oscillometry), and Clinical Adjudication (centralized endpoint committee platform). Supporting capabilities include Trial Enablement software, AI Solutions (120+ models across 600+ trials), and Hybrid Trials services. The platform operates across 100+ countries in 100+ languages, supporting over 30,000 trials and approximately 70% of FDA and EMA new drug approvals since 2015.

Product and service14 records
1Cardiac Solutions
CategoryCardiac Safety Solutions
Description

Global-ready cardiac safety and efficacy endpoint solutions for all phases of clinical trials, including centralized ECG collection, arrhythmia analysis, blood pressure monitoring, and regulatory consulting. Supports more than 13,800 trials globally and more than 580 new drug approvals through cardiac solutions alone.

2eCOA (Electronic Clinical Outcome Assessment)
CategoryElectronic Clinical Outcome Assessment
Description

Comprehensive electronic clinical outcome assessment platform supporting electronic patient-reported outcomes (ePRO), clinician-reported outcomes (eClinRO), and performance outcomes (ePerfO) across decentralized, hybrid, and site-based trials in 120+ countries.

3Medical Imaging
CategoryMedical Imaging Core Lab
Description

World-leading centralized medical imaging core lab services for clinical trials with SMART technology suite processing images from electronic transfer through independent analysis. Supports more than 5,000 imaging studies across CT, MRI, endoscopy, and other modalities.

4Precision Motion
CategoryWearable Motion Sensors
Description

Complete solution for measuring objective digital endpoints of mobility using Opal® wearable sensor technology, including Opal V2C® for clinical trials and Opal V2R® for research applications. Predictive of fall risk in Parkinson's patients with 84-92% accuracy up to two years in advance.

5Respiratory Solutions
CategoryRespiratory Solutions
Description

Comprehensive respiratory endpoint solutions generating high-quality pulmonary function data through site-based spirometry, virtual home spirometry, cough/lung sound assessment, DLCO, and oscillometry. Includes FDA-cleared SpiroSphere® device with wireless ECG.

6Clinical Adjudication
CategoryClinical Adjudication Platform
Description

Centralized, cloud-based clinical endpoint adjudication platform with real-time case routing, automated workflows, AI-driven redaction, and discordance detection. Supports 15,000+ active users across 61 countries.

7Trial Enablement
CategoryClinical Trial Software
Description

Cloud-native technologies and clinical trial software for participant screening, data collection, cleaning, QC, and assessment including Eligibility Solution, Reporting & Analytics, and Source Document Manager.

8Artificial Intelligence (AI) Solutions
CategoryAI Platform
Description

AI-enabled clinical trial solutions including more than 120 AI models deployed across 600+ active trials. Capabilities span vocal biomarkers, Image Redact AI, AI-enabled spirometry insights, and Study Insight Analytics, certified to ISO 42001:2023.

9Hybrid Trials
CategoryDecentralized/Hybrid Trial Services
Description

Endpoint technology and services for virtual or hybrid clinical trials combining on-site and remote data collection using connected devices and decentralized trial capabilities across 100+ countries.

10Suicidal Ideation Assessment (eC-SSRS)
CategoryClinical Outcome Assessment
Description

Electronic Columbia-Suicide Severity Rating Scale (C-SSRS) for monitoring suicidal ideation and behavior in clinical trials. Includes patient-reported ePRO and clinician-led eClinRO options with real-time alerts to clinicians; exclusive clinical trial licensing.

11Rater, Participant and Caregiver Training
CategoryTraining Services
Description

Comprehensive training solutions including PANSS rater training, placebo response reduction training, and participant/caregiver training. Trained 41k+ clinical site raters and 125k+ participants/caregivers, including 8 of top 10 biopharmaceutical companies utilizing rater training services.

12Phase I/TQT Cardiac Assessment (EPQT)
CategoryCardiac Safety Solutions
Description

Early Precision QT (EPQT) methodology for cost-effective QT assessments in Phase I studies, enabling earlier cardiac safety decisions and potential TQT waiver qualification under ICH E14 guidelines.

13eCOA Swift (Early Phase Oncology)
CategoryElectronic Clinical Outcome Assessment
Description

Fast, cost-effective eCOA solution for early phase oncology trials with setup in as little as 2 weeks. Delivers near-real-time tolerability monitoring and 90%+ compliance rates.

14eCOA Rapid Start (Assessment Catalog)
CategoryElectronic Clinical Outcome Assessment
Description

Pre-validated and configured eCOA assessments enabling trial setup from kick-off to UAT in as little as 6 weeks. Features 1,000+ pre-validated, version-controlled assessments with 2.8M+ patients engaged.

Scale indicator17 records

Each record includes

Type, Value, Description, Source

Partnership6 partners
Strategic tierMinorTypeStrategic or Co-development PartnerAnnounced on2025-10-06
Description

Collaboration to advance Parkinson's disease research using Clario's Opal wearable sensor system. First participant enrolled in study to validate fall risk prediction capabilities.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2025-05-06
Description

Clario completed acquisition of WCG's electronic clinical outcome assessment (eCOA) business, enhancing capabilities in neuroscience clinical trial data collection and analysis. The acquisition expanded expertise in neuroscience, psychiatry, and rare diseases.

Strategic tierCoreTypeTechnology or IntegrationAnnounced on2025-03-17
Description

Clario and PathAI announced collaboration to deliver an integrated solution for gastrointestinal (GI) clinical trials, combining Clario's endpoint expertise with PathAI's AI-powered pathology analysis.

Strategic tierMinorTypeStrategic or Co-development PartnerAnnounced on2024-08-13
Description

Clario joined forces with Mobilise-D to advance Digital Mobility Outcomes in clinical trials, combining expertise in wearable sensors and mobility assessment.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2024-04-02
Description

Clario acquired ArtiQ, an AI-powered software company specializing in respiratory solutions. The acquisition expanded Clario's respiratory solutions portfolio and AI capabilities for respiratory testing, enhancing quality and efficiency of clinical trial data analysis.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2024-03-17
Description

Clario acquired NeuroRx, an imaging analysis provider specializing in neurological therapies including multiple sclerosis. This strengthened Clario's capabilities in neuroscience imaging.

Recent move7 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight7 records

Each record includes

Type, Description

Peers10 records
TypeBroad incumbent
Description

Parexel is a global CRO with endpoint, biostatistics, and clinical pharmacology services that overlap with Clario's Phase I/cardiac safety and statistical analysis offerings, particularly in early-phase and regulatory strategy engagements.

TypeBroad incumbent
Description

IQVIA is the largest global CRO with embedded eClinical/endpoint technology capabilities. It competes with Clario on integrated endpoint delivery, particularly through its R&D Solutions segment, while also being a customer/channel for some endpoint services.

TypeBroad incumbent
Description

ICON is a top-3 global CRO that delivers endpoint, imaging, and eCOA-adjacent services. It is both a competitor for integrated trial delivery and a customer of endpoint technology.

TypeDirect peer
Description

BioTelemetry, acquired by Philips, provides cardiac monitoring services including MCT and Holter for clinical trials, directly competing with Clario's Cardiac Solutions portfolio (arrhythmia, ECG, ambulatory BP).

TypeDirect peer
Description

Signant Health (formerly CRF Health and Bracket) provides eCOA, rater training, and clinical supply solutions, directly competing with Clario's eCOA and neuroscience offerings for CNS and rare disease trials.

TypeDirect peer
Description

Veeva's Vault CTMS, Vault EDC, and Vault CDB compete directly with Clario's trial enablement and clinical data infrastructure offerings. Veeva's life-sciences cloud software stack overlaps Clario's enterprise SaaS GTM into pharma/biotech sponsors.

TypeDirect peer
Description

Medidata's Rave platform is a leading EDC/eCOA/Imaging/CTMS suite widely used in clinical trials. It is the closest direct competitor to Clario's eCOA and Trial Enablement offerings, with overlapping endpoints, customers (large pharma/biotech), and a comparable SaaS-style enterprise GTM.

TypeEmerging player
Description

Medable focuses on decentralized clinical trial (DCT) platform technology, overlapping with Clario's hybrid trial, eCOA Live, and connected-device initiatives. Medable is a more focused emerging competitor in DCT enablement.

TypeEmerging player
Description

Castor offers an eClinical platform (EDC, ePRO, eConsent) targeting academic and emerging biotech sponsors. It competes with Clario's eCOA and trial enablement offerings in the small-to-mid sponsor segment.

TypeBroad incumbent
Description

Oracle's Clinical One platform offers unified EDC, RTSM, and eCOA capabilities that compete with Clario's endpoint platform, particularly for large Phase III programs and sponsors standardizing on Oracle infrastructure.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat6 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers1 record

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment5 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile3 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

Integration7 records

Each record includes

Title, Type, Description, Source

AI capability12 records

Each record includes

Type, Description, Source

AI maturity
App detail

Has app

Feature7 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles14 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

Subsidiaries3 records

Each record includes

Name, Acquired on, Relationship type, Type, Business focus

Compliance5 records

Each record includes

Name, Class, Description

Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds2 records

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors3 records

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A3 records

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Clario

Clinical Trial Endpoint Technologyclario.com

Clario is a clinical trial endpoint technology company providing cloud-native eCOA, cardiac safety, medical imaging, precision motion, and respiratory solutions to pharmaceutical, biotech, and CRO sponsors across 100+ countries, supporting 70% of FDA/EMA novel drug approvals since 2015.

What Clario does

Clario is a clinical trial endpoint technology company that provides data and technology solutions for drug and medical device approvals across pharmaceutical, biotechnology, and Contract Research Organization (CRO) customers. Formed in 2021 through the merger of ERT (eResearchTechnology) and Bioclinica, the company operates a cloud-native integrated platform spanning six core product lines: Cardiac Solutions (ECG, arrhythmia, blood pressure, Phase I/TQT assessment); eCOA (electronic clinical outcome assessments including neuroscience, oncology, rater training, and the eC-SSRS for suicidal ideation monitoring); Medical Imaging (centralized core lab with AI-powered redaction and SMART Submit); Precision Motion (Opal V2R/V2C wearable sensors for digital mobility endpoints); Respiratory Solutions (SpiroSphere, home spirometry, oscillometry); and Clinical Adjudication (centralized endpoint committee platform with 15,000+ active users across 61 countries). The platform is supported by Trial Enablement software and AI Solutions with 120+ proprietary AI models deployed across 600+ active trials. Notable proprietary technologies include the FDA-cleared SpiroSphere with wireless ECG, the EPQT (Early Precision QT) methodology enabling potential TQT waiver qualification, and Opal sensors capable of predicting fall risk in Parkinson's patients with 84-92% accuracy.

Clario's go-to-market is enterprise field sales targeting pharmaceutical sponsors, biotech companies, and CROs globally, with study-by-study pricing that scales with therapeutic area, endpoints, geographies, languages, patient volume, and study duration. Sales cycles are long and technically complex, requiring deep scientific and regulatory expertise. The company has supported over 30,000 clinical trials across more than 100 countries with translations in over 100 languages, contributing to approximately 70% of FDA and EMA novel drug approvals since 2015 (700+ approvals). It maintains 70,000+ active trial sites, ships 136,000 validated devices per year through logistics hubs in the US, EU, and Japan, and has engaged 2.8 million+ patients through its eCOA Rapid Start catalog and 500,000+ patients in eCOA neuroscience trials.

Revenue derives primarily from clinical trial endpoint services billed study-by-study under multi-year enterprise agreements, supplemented by technology licensing and platform access. 2025 revenue was projected at approximately $1.25 billion prior to Clario's acquisition by Thermo Fisher Scientific, completed in March 2026 for $8.875 billion in cash plus up to $525 million in earnout payments — representing an exit for private equity sponsors Astorg, Cinven, Nordic Capital, and Novo Holdings. Post-acquisition, Clario operates as a subsidiary within Thermo Fisher's clinical research services segment.

Clario firmographics

Firmographics
Name
Clario
Legal name
Clario
Website
https://clario.com
Company type
Private
Founded year
2021
Operating status
Acquired
Headcount range
1,001–5,000 employees
Short description
Clario is a clinical trial endpoint technology company providing cloud-native eCOA, cardiac safety, medical imaging, precision motion, and respiratory solutions to pharmaceutical, biotech, and CRO sponsors across 100+ countries, supporting 70% of FDA/EMA novel drug approvals since 2015.
Ownership category
akta.pro rank

Clario industry classification

Industry
Product category
Clinical Trial Endpoint Technology
NAICS
Computer Systems Design and Related Services (54151), Medical and Diagnostic Laboratories (6215), Analytical Laboratory Instrument Manufacturing (334516)
SIC
Services-Prepackaged Software (7372), Services-Medical Laboratories (8071), Surgical & Medical Instruments & Apparatus (3841)
akta.pro primary industry
Clinical Trial Informatics (EDC/CTMS/eCOA/eTMF) (HLAGAJAM)
akta.pro secondary industries
Clinical CROs (Phase I–IV) (HLAGAAAA), Clinical Data Management, Biostatistics & Statistical Programming CROs (HLAGAAAF)

Keywords

  • Clinical trial endpoints
  • Cardiac safety monitoring
  • Electronic clinical outcomes
  • Medical imaging core lab
  • Clinical trial technology

Where Clario is headquartered

Location

Headquarters

HQ city
Philadelphia
HQ country
United States
HQ region
North America

Offices3 records

Markets served

Clario business model

Business model
GTM type
B2B
Offering type
Software
Cost components
Personnel, Technology or R&D, Operations, Infrastructure, Marketing or Sales

Revenue model

  1. Clinical Trial Endpoint Solutions: Clario generates revenue by providing endpoint data solutions to pharmaceutical and biotech companies conducting clinical trials. Services are priced study-by-study based on complexity, scope, geographic reach, and duration. Revenue projected at approximately $1.25 billion in 2025 prior to acquisition by Thermo Fisher.
  2. Technology Licensing and Platform Access: Revenue from licensing proprietary technology platforms, AI models, and specialized assessment tools to clinical trial sponsors and CROs.

Pricing tiers

ModelBillingPrice
SubscriptionMulti-year contractEnterprise study-based pricing

Go-to-market motion2 records

Distribution channels1 record

Marketing channels7 records

Clario product offering

Product offering

Core offering

Clario provides technology-enabled endpoint data solutions for clinical trials that collect, process, and analyze data used to support drug and medical device approvals. Its offerings span six core endpoint categories: Cardiac Solutions (centralized ECG, arrhythmia analysis, blood pressure, Phase I/TQT assessment), eCOA (electronic patient-, clinician-, and performance-reported outcomes including neuroscience modules), Medical Imaging (centralized imaging core lab with SMART Submit platform), Precision Motion (Opal® wearable sensors for mobility endpoints), Respiratory Solutions (spirometry, oscillometry, SpiroSphere® device), and Clinical Adjudication (centralized endpoint committee platform). Supporting capabilities include Trial Enablement software, Hybrid Trials services, and an AI platform with 120+ models, all delivered globally across 100+ countries.

Product overview

Clario is a clinical trial endpoint technology company offering a comprehensive platform of endpoint solutions for clinical trials. The portfolio includes six core products: Cardiac Solutions (ECG, arrhythmia, blood pressure monitoring with regulatory consulting), eCOA (electronic clinical outcome assessments including neuroscience, oncology, and specialized modules like Swift, Rapid Start, and training), Medical Imaging (centralized core lab services with SMART technology), Precision Motion (Opal® wearable sensors for mobility), Respiratory Solutions (spirometry, home testing, oscillometry), and Clinical Adjudication (centralized endpoint committee platform). Supporting capabilities include Trial Enablement software, AI Solutions (120+ models across 600+ trials), and Hybrid Trials services. The platform operates across 100+ countries in 100+ languages, supporting over 30,000 trials and approximately 70% of FDA and EMA new drug approvals since 2015.

Differentiator

Problem solved

Functional benefit

Brands

  • eResearchTechnology (ERT): Legacy brand for cardiac safety solutions, part of Clario's portfolio
  • Bioclinica
  • Opal V2R
  • Opal System
  • SpiroSphere
  • eC-SSRS
  • SMART Submit
  • Virgil Academy
  • Virgil University
  • SafePatient ECG

Products and services

  • Cardiac Solutions Global-ready cardiac safety and efficacy endpoint solutions for all phases of clinical trials, including centralized ECG collection, arrhythmia analysis, blood pressure monitoring, and regulatory consulting. Supports more than 13,800 trials globally and more than 580 new drug approvals through cardiac solutions alone.
  • eCOA (Electronic Clinical Outcome Assessment) Comprehensive electronic clinical outcome assessment platform supporting electronic patient-reported outcomes (ePRO), clinician-reported outcomes (eClinRO), and performance outcomes (ePerfO) across decentralized, hybrid, and site-based trials in 120+ countries.
  • Medical Imaging World-leading centralized medical imaging core lab services for clinical trials with SMART technology suite processing images from electronic transfer through independent analysis. Supports more than 5,000 imaging studies across CT, MRI, endoscopy, and other modalities.
  • Precision Motion Complete solution for measuring objective digital endpoints of mobility using Opal® wearable sensor technology, including Opal V2C® for clinical trials and Opal V2R® for research applications. Predictive of fall risk in Parkinson's patients with 84-92% accuracy up to two years in advance.
  • Respiratory Solutions Comprehensive respiratory endpoint solutions generating high-quality pulmonary function data through site-based spirometry, virtual home spirometry, cough/lung sound assessment, DLCO, and oscillometry. Includes FDA-cleared SpiroSphere® device with wireless ECG.
  • Clinical Adjudication Centralized, cloud-based clinical endpoint adjudication platform with real-time case routing, automated workflows, AI-driven redaction, and discordance detection. Supports 15,000+ active users across 61 countries.
  • Trial Enablement Cloud-native technologies and clinical trial software for participant screening, data collection, cleaning, QC, and assessment including Eligibility Solution, Reporting & Analytics, and Source Document Manager.
  • Artificial Intelligence (AI) Solutions AI-enabled clinical trial solutions including more than 120 AI models deployed across 600+ active trials. Capabilities span vocal biomarkers, Image Redact AI, AI-enabled spirometry insights, and Study Insight Analytics, certified to ISO 42001:2023.
  • Hybrid Trials Endpoint technology and services for virtual or hybrid clinical trials combining on-site and remote data collection using connected devices and decentralized trial capabilities across 100+ countries.
  • Suicidal Ideation Assessment (eC-SSRS) Electronic Columbia-Suicide Severity Rating Scale (C-SSRS) for monitoring suicidal ideation and behavior in clinical trials. Includes patient-reported ePRO and clinician-led eClinRO options with real-time alerts to clinicians; exclusive clinical trial licensing.
  • Rater, Participant and Caregiver Training Comprehensive training solutions including PANSS rater training, placebo response reduction training, and participant/caregiver training. Trained 41k+ clinical site raters and 125k+ participants/caregivers, including 8 of top 10 biopharmaceutical companies utilizing rater training services.
  • Phase I/TQT Cardiac Assessment (EPQT) Early Precision QT (EPQT) methodology for cost-effective QT assessments in Phase I studies, enabling earlier cardiac safety decisions and potential TQT waiver qualification under ICH E14 guidelines.
  • eCOA Swift (Early Phase Oncology) Fast, cost-effective eCOA solution for early phase oncology trials with setup in as little as 2 weeks. Delivers near-real-time tolerability monitoring and 90%+ compliance rates.
  • eCOA Rapid Start (Assessment Catalog) Pre-validated and configured eCOA assessments enabling trial setup from kick-off to UAT in as little as 6 weeks. Features 1,000+ pre-validated, version-controlled assessments with 2.8M+ patients engaged.

Quantifiable outcome

  • 70% of FDA and EMA novel drug approvals since 2015 supported by Clario's platform
  • +6 more outcomes

Companies that use Clario

Customer profile

Named customers1 record

Segments5 records

Ideal customer profiles3 records

Clario technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Integration7 records

AI capability12 records

Feature7 records

Clario partnerships and signals

Strategic signal

Partnerships

Six partnerships are on record, tiered minor and core.

  • University of Oxford (NeuroMetrology Lab)minorStrategic or Co-development Partner · 6 October 2025Collaboration to advance Parkinson's disease research using Clario's Opal wearable sensor system. First participant enrolled in study to validate fall risk prediction capabilities.
  • WCG (eCOA Business)coreStrategic or Co-development Partner · 6 May 2025Clario completed acquisition of WCG's electronic clinical outcome assessment (eCOA) business, enhancing capabilities in neuroscience clinical trial data collection and analysis. The acquisition expanded expertise in neuroscience, psychiatry, and rare diseases.
  • PathAIcoreTechnology or Integration · 17 March 2025Clario and PathAI announced collaboration to deliver an integrated solution for gastrointestinal (GI) clinical trials, combining Clario's endpoint expertise with PathAI's AI-powered pathology analysis.
  • Mobilise-DminorStrategic or Co-development Partner · 13 August 2024Clario joined forces with Mobilise-D to advance Digital Mobility Outcomes in clinical trials, combining expertise in wearable sensors and mobility assessment.
  • ArtiQcoreStrategic or Co-development Partner · 2 April 2024Clario acquired ArtiQ, an AI-powered software company specializing in respiratory solutions. The acquisition expanded Clario's respiratory solutions portfolio and AI capabilities for respiratory testing, enhancing quality and efficiency of clinical trial data analysis.
  • NeuroRxcoreStrategic or Co-development Partner · 17 March 2024Clario acquired NeuroRx, an imaging analysis provider specializing in neurological therapies including multiple sclerosis. This strengthened Clario's capabilities in neuroscience imaging.

Scale indicators17 records

Recent moves7 records

Expansion highlights7 records

Clario competitors and assessment

Company assessment

Broad incumbents

  • Parexel: Parexel is a global CRO with endpoint, biostatistics, and clinical pharmacology services that overlap with Clario's Phase I/cardiac safety and statistical analysis offerings, particularly in early-phase and regulatory strategy engagements.
  • IQVIA: IQVIA is the largest global CRO with embedded eClinical/endpoint technology capabilities. It competes with Clario on integrated endpoint delivery, particularly through its R&D Solutions segment, while also being a customer/channel for some endpoint services.
  • ICON plc: ICON is a top-3 global CRO that delivers endpoint, imaging, and eCOA-adjacent services. It is both a competitor for integrated trial delivery and a customer of endpoint technology.
  • Oracle Health Sciences (Clinical One): Oracle's Clinical One platform offers unified EDC, RTSM, and eCOA capabilities that compete with Clario's endpoint platform, particularly for large Phase III programs and sponsors standardizing on Oracle infrastructure.

Direct peers

  • BioTelemetry (Philips): BioTelemetry, acquired by Philips, provides cardiac monitoring services including MCT and Holter for clinical trials, directly competing with Clario's Cardiac Solutions portfolio (arrhythmia, ECG, ambulatory BP).
  • Signant Health: Signant Health (formerly CRF Health and Bracket) provides eCOA, rater training, and clinical supply solutions, directly competing with Clario's eCOA and neuroscience offerings for CNS and rare disease trials.
  • Veeva Systems: Veeva's Vault CTMS, Vault EDC, and Vault CDB compete directly with Clario's trial enablement and clinical data infrastructure offerings. Veeva's life-sciences cloud software stack overlaps Clario's enterprise SaaS GTM into pharma/biotech sponsors.
  • Medidata Solutions (Dassault Systèmes): Medidata's Rave platform is a leading EDC/eCOA/Imaging/CTMS suite widely used in clinical trials. It is the closest direct competitor to Clario's eCOA and Trial Enablement offerings, with overlapping endpoints, customers (large pharma/biotech), and a comparable SaaS-style enterprise GTM.

Emerging players

  • Medable: Medable focuses on decentralized clinical trial (DCT) platform technology, overlapping with Clario's hybrid trial, eCOA Live, and connected-device initiatives. Medable is a more focused emerging competitor in DCT enablement.
  • Castor: Castor offers an eClinical platform (EDC, ePRO, eConsent) targeting academic and emerging biotech sponsors. It competes with Clario's eCOA and trial enablement offerings in the small-to-mid sponsor segment.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat6 records

Key risks6 records

Key highlights7 records

Customer concentration

Clario social profiles

Digital presence

Clario compliance and trust

Trust signal

Compliance5 records

Clario financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Clario leadership team

Management profile

Number of profiles

Profiles14 records

Clario subsidiaries and ownership

Company hierarchy

Subsidiaries3 records

Clario funding detail

Funding detail

Funding overview

Funding rounds2 records

Investors3 records

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

Clario M&A and investment

M&A and investment

M&A3 records

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about Clario

What does Clario do?

Clario provides technology-enabled endpoint data solutions for clinical trials that collect, process, and analyze data used to support drug and medical device approvals. Its offerings span six core endpoint categories: Cardiac Solutions (centralized ECG, arrhythmia analysis, blood pressure, Phase I/TQT assessment), eCOA (electronic patient-, clinician-, and performance-reported outcomes including neuroscience modules), Medical Imaging (centralized imaging core lab with SMART Submit platform), Precision Motion (Opal® wearable sensors for mobility endpoints), Respiratory Solutions (spirometry, oscillometry, SpiroSphere® device), and Clinical Adjudication (centralized endpoint committee platform). Supporting capabilities include Trial Enablement software, Hybrid Trials services, and an AI platform with 120+ models, all delivered globally across 100+ countries.

Is Clario a public or private company?

Clario is a private company. It is classified as corporate owned and is currently acquired.

When was Clario founded?

Clario was founded in 2021. It employs 1,001 to 5,000 people.

Where is Clario based?

Clario is headquartered in Philadelphia, United States, in the North America region.

How does Clario make money?

Two revenue lines are on record. Clinical Trial Endpoint Solutions are the primary driver. The others are technology Licensing and Platform Access.

Who are Clario's main competitors?

Broad incumbents on record are Parexel, IQVIA, ICON plc and Oracle Health Sciences (Clinical One). Direct peers are BioTelemetry (Philips), Signant Health, Veeva Systems and Medidata Solutions (Dassault Systèmes). Emerging players are Medable and Castor.

Does Clario have an API?

No public API is recorded for Clario.

What industry is Clario in?

Clario's product category is Clinical Trial Endpoint Technology. Its primary akta.pro industry code is HLAGAJAM, Clinical Trial Informatics (EDC/CTMS/eCOA/eTMF), with a secondary code of HLAGAAAA, Clinical CROs (Phase I–IV). Its NAICS code is 54151 and its SIC code is 7372.

Unlock the full company data

50 free credits on sign-up, no credit card required.

Contact sales
Live signals
PR NewswireClinical Trials Services Market worth $97.41 billion by 2031 - Exclusive Report by MarketsandMarkets™The clinical trials services market is projected to grow from $66.20 billion in 2026 to $97.41 billion by 2031, an 8.0% CAGR. North America holds the largest share at ~45%, and the biologics segment is expected to see the highest growth. Hybrid delivery models and AI-enabled operations are driving demand.PR NewswireOptimize Obesity Development: Endpoint Strategies for Early-phase Innovation to Late-phase Differentiation, Upcoming Webinar Hosted by XtalksXtalks will host a free webinar on endpoint strategies for obesity drug development, covering patient-reported outcomes, glucose monitoring, cardiac assessments, and medical imaging. The event aims to help sponsors generate stronger evidence for regulatory review and product differentiation. It is scheduled for September 17, 2026, with speakers from Clario and other organizations.Insider Trading & Hedge Fund DataCan A New Vitiligo Registry Move The Needle For Thermo Fisher (TMO)? - Insider MonkeyThermo Fisher Scientific announced on July 29 that it launched the PPD CorEvitas Vitiligo Registry on July 14 to monitor treatment responses in vitiligo patients, emphasizing its real-world data segment. The company continues to expand through acquisitions, including Clario Holdings and Solventum’s filtration unit, aiming to enhance its data and evidence services.AIM Media HouseAI-Driven Demand Fuels Thermo Fisher's Earnings Beat and Raised OutlookThermo Fisher Scientific reported second-quarter 2026 adjusted earnings of $6.03 per share on $11.99 billion in revenue, beating analyst estimates and raising its full-year guidance to $47.4–$48.1 billion in revenue and $24.93–$25.33 in adjusted EPS, with shares rising 8.97%. The company attributed the beat to AI-driven demand for its new instruments and software, including AI-enabled mass spectrometers launched at a June conference, as pharmaceutical companies increase AI-based drug discovery spending that funds Thermo Fisher's core business. The company closed its acquisition of clinical data company Clario in March and returned $1.2 billion to shareholders in the quarter.PR NewswirePrecision Neurology Made Practical: Faster Development Through Biomarkers and Real-World Insight, Upcoming Webinar Hosted by XtalksXtalks is hosting a free webinar on July 15, 2026, focused on accelerating precision neurology drug development through biomarker strategies, patient identification approaches, and real-world evidence integration. The webinar will feature speakers from PPD Clinical Research Services, Thermo Fisher Scientific, and Clario discussing how these approaches can improve study efficiency, refine trial design, and support commercialization planning. Registration is open for the live event, which is part of Xtalks' life science industry knowledge-sharing platform.PR NewswireRisk-Based Monitoring in Clinical Trials: Improve Oversight Through Intelligent Review of Digital Endpoint Data, Upcoming Webinar Hosted by XtalksXtalks has announced a free webinar on Risk-Based Monitoring in clinical trials, scheduled for June 11, 2026, featuring experts from Clario. The webinar will cover how AI-supported and expert-validated data monitoring can improve endpoint integrity and proactively minimize risk in clinical trials through centralized data review and advanced analytics.Investing.comhttps://in.investing.com/news/swot-analysis/thermo-fisher-scientifics-swot-analysis-stock-navigates-growth-amid-strategic-shifts-93CH-5419863Thermo Fisher Scientific is undergoing a strategic transformation marked by a $9 billion acquisition of Clario announced in October 2025, paired with significant management changes including the departures of COO Michel Lagarde and EVP Frederick Lowery in January 2026. The company reported solid third-quarter 2025 results with 4% core growth in Analytical Instruments but has faced conservative guidance adjustments, reducing its fiscal year 2026 growth framework from 3%-6% to 3%-4%. Analysts maintain divided outlooks with price targets ranging from $625 to $750 while monitoring for catalysts that could drive upside as biopharma spending normalizes.Investing.comhttps://www.investing.com/news/swot-analysis/thermo-fisher-scientifics-swot-analysis-stock-navigates-growth-amid-strategic-shifts-93CH-4703274Thermo Fisher Scientific Inc. announced in January 2026 a management shake-up including the departure of Chief Operating Officer Michel Lagarde and Executive Vice President Frederick Lowery, with Gianluca Pettiti promoted to President and COO. The company also disclosed in October 2025 its planned acquisition of Clario, a provider of electronic Clinical Outcome Assessments and AI solutions for clinical trials, valued at approximately $9 billion. Thermo Fisher reported solid third-quarter 2025 results with 4% core growth in Analytical Instruments and $45.2 billion in trailing twelve-month revenue, while providing conservative fiscal year 2026 guidance of 3% to 4% growth amid improving biopharma spending conditions.openPR.comFuture Perspectives: Key Trends Shaping the eCOA, eSource, and Clinical Trials Market Until 2030The eCOA, eSource, and clinical trials market is projected to reach $81.46 billion by 2030, growing at a compound annual growth rate of 9.8%, driven by AI-powered data validation, decentralized trial models, patient-centric studies, and increased adoption of cloud-based clinical systems. In August 2023, Sitero LLC acquired Clario's eClinical technology suite, enabling Sitero to expand its offerings in eCOA, eSource, and clinical trials solutions. Additionally, THREAD Research launched an expanded global eCOA library in September 2023 featuring over 540 pre-validated questionnaires, which can reduce implementation time and lower development costs by up to 54%.FierceBiotechThermo Fisher sees higher Q1 earnings amid strong biopharma demandThermo Fisher Scientific reported a strong Q1 with revenues rising 6% to $11.01 billion and adjusted EPS of $5.44, driven by robust biopharma demand and the completion of its $9 billion acquisition of clinical trial data company Clario. The company's laboratory products and biopharma services segment grew 7% to $6.04 billion, and it raised its 2026 revenue guidance to $47.3–48.1 billion. CEO Marc Casper highlighted AI as a long-term growth opportunity, citing a partnership with Nvidia to build autonomous laboratory infrastructure.