MedAvante
MedAvante is a clinical trial technology and services company providing technology-enabled signal detection and endpoint solutions — including eCOA, cardiac safety, imaging, motion, and respiratory — to pharmaceutical, biotech, and CRO sponsors across global trials.
- Company typePrivate
- Founded2002
- HeadquartersHackensack, United States
- Headcount101–250
- GTM typeB2B
- OfferingSoftware
What MedAvante does
MedAvante, founded in 2002 and headquartered in Hackensack, New Jersey, is a clinical trial technology and services company focused on technology-enabled signal detection and endpoint solutions for drug development. The company serves large pharmaceutical sponsors, biotechnology firms, and contract research organizations (CROs) across all phases of clinical trials, deploying its platform across more than 100 countries with translations in over 100 languages. MedAvante has supported more than 30,000 clinical trials and has contributed to 700+ FDA and EMA new drug approvals, including 70% of FDA and EMA approvals since 2015.
The company's product portfolio spans eCOA (Electronic Clinical Outcome Assessment), cardiac safety solutions including ECG and arrhythmia analysis, medical imaging core lab services, the Opal V2R precision motion wearable sensor platform, and respiratory solutions including site-based and virtual spirometry. Underlying the product suite is a cloud-native trial enablement layer for screening, eligibility, source document management, and analytics. MedAvante also holds exclusive distribution rights to the eC-SSRS electronic Columbia Suicide Severity Rating Scale for self-reported suicidal ideation monitoring in CNS trials, and has launched Image Redact AI to automate the redaction of patient identifiers in imaging, video, and PDF artifacts.
MedAvante operates an enterprise sales model targeting pharma, biotech, and CRO buyers with quote-based, multi-year master agreements covering site-based, hybrid, and decentralized clinical trial deployments. In 2026, the company was acquired by Thermo Fisher Scientific as part of the broader acquisition of Clario Holdings Inc., which had integrated MedAvante's endpoint technology platform. The company's go-to-market combines direct enterprise engagement with content-led demand generation through its corporate website, scientific publications, industry conferences, and webinars aimed at clinical operations and biostatistics buyers.
MedAvante firmographics
Firmographics- Name
- MedAvante
- Website
- https://medavante.com
- Company type
- Private
- Founded year
- 2002
- Operating status
- Operating
- Headcount range
- 101–250 employees
- Short description
- MedAvante is a clinical trial technology and services company providing technology-enabled signal detection and endpoint solutions — including eCOA, cardiac safety, imaging, motion, and respiratory — to pharmaceutical, biotech, and CRO sponsors across global trials.
- Ownership category
- akta.pro rank
MedAvante industry classification
Industry- Product category
- Clinical Trial Endpoint Technology
- NAICS
- Other Scientific and Technical Consulting Services (541690), Medical Equipment and Supplies Manufacturing (3391)
- SIC
- Services-Prepackaged Software (7372), Services-Misc Health & Allied Services, Nec (8090)
- akta.pro primary industry
- eCOA/ePRO/eDiary & Patient-Facing Data Collection (HLACAOAB)
- akta.pro secondary industries
- Clinical Trial Informatics (EDC/CTMS/eCOA/eTMF) (HLAGAJAM), Clinical Trial Monitoring Support (On-site/Remote) (HLAGACAG), Site & Investigator Platforms (Site Payments, Feasibility, Activation) (HLACAOAJ)
Keywords
Where MedAvante is headquartered
LocationHeadquarters
- HQ city
- Hackensack
- HQ country
- United States
- HQ region
- North America
Markets served
MedAvante business model
Business model- GTM type
- B2B
- Offering type
- Software
- Cost components
- Personnel, Technology or R&D, Operations, Marketing or Sales, Infrastructure
Distribution channels1 record
Marketing channels6 records
MedAvante product offering
Product offeringCore offering
MedAvante provides technology-enabled clinical trial endpoint solutions for pharmaceutical, biotechnology, and CRO sponsors. Its offerings span electronic clinical outcome assessments (eCOA), cardiac safety monitoring, medical imaging core lab services, precision motion wearables (Opal System), respiratory function testing, and cloud-native trial enablement software. These solutions are delivered across site-based, hybrid, and decentralized clinical trial models in over 100 countries.
Differentiator
Problem solved
Functional benefit
Products and services
- Cardiac Safety Solutions Cardiac safety and efficacy endpoint solutions including ECG monitoring, arrhythmia analysis, blood pressure data collection, and Phase I/TQT cardiac assessment for all trial phases, delivered to pharmaceutical, biotech, and CRO sponsors globally.
- eCOA (Electronic Clinical Outcome Assessment) Digital collection of patient-reported outcomes, clinician-reported outcomes, observer-reported outcomes, and performance outcomes for clinical trials, including neuroscience, early-phase oncology, rapid start assessment catalogs, science services, and rater training offerings.
- Medical Imaging Core Lab Services Comprehensive medical imaging core lab services including CT scans, endoscopy, MRIs and other modalities, backed by over 5,000 imaging studies and an experienced imaging science team with global key opinion leaders.
- Precision Motion / Opal System Wearable sensor technology for measuring objective digital endpoints of mobility, featuring the research-grade Opal V2R wearable sensor and supported by 750+ scientific publications reflecting its technical and clinical applications.
- Respiratory Solutions Pulmonary function testing including site-based spirometry, virtual home spirometry, cough and lung sounds assessment, diffusing capacity (DLCO), and oscillometry, generating reliable pulmonary data with low variability and high patient compliance.
- Trial Enablement Technology Cloud-native technologies and clinical trial software for participant screening, eligibility management, business intelligence analytics, and source document management, supporting site-based, hybrid, and decentralized clinical trials.
- Image Redact AI AI-powered solution that automatically redacts sensitive patient identifiers from videos, photos, and PDFs to support privacy and regulatory compliance in clinical trial imaging workflows.
- eC-SSRS (electronic Columbia Suicide Severity Rating Scale) Exclusive self-reported electronic Columbia Suicide Severity Rating Scale solution for monitoring suicidal ideation and behavior in clinical trials.
Quantifiable outcome
- 70% of FDA and EMA new drug approvals since 2015
- +3 more outcomes
Companies that use MedAvante
Customer profileSegments3 records
Ideal customer profiles3 records
MedAvante technology and API
TechnologyTechnology focussed Yes
API detail
- Has API
- No
- API docs
- API detail
Core technology
AI maturity
App detail
Feature8 records
MedAvante partnerships and signals
Strategic signalScale indicators8 records
Recent moves6 records
Expansion highlights6 records
MedAvante competitors and assessment
Company assessmentDirect peers
- Veeva Systems: Veeva provides the Vault CTMS, EDC, and ePRO platform used across the life sciences industry. It is one of the closest software-direct comparables to MedAvante's eCOA and trial enablement technology stack.
- Signant Health: Signant Health (formed from CRF Health and Bracket) is a focused eCOA, patient engagement, and clinical outcome assessment provider. It is a direct competitor to MedAvante's eCOA franchise, particularly in CNS and rare disease trials.
Broad incumbents
- Parexel: Parexel is a global CRO with extensive clinical technology and decentralized trial offerings following its private-equity ownership. It competes with MedAvante on eCOA, cardiac safety, and integrated trial delivery.
- IQVIA: IQVIA is the largest global CRO and offers clinical trial technology, eCOA, and real-world evidence services. It competes head-to-head with MedAvante on endpoint solutions while bundling them with full-service CRO delivery to large pharma sponsors.
- Labcorp Drug Development (Fortrea): Fortrea (spun out from Labcorp) is a major global CRO with central laboratory, imaging, and eCOA capabilities. It is a broad incumbent that competes with MedAvante across multiple endpoint modalities as part of integrated CRO contracts.
- ICON plc: ICON is a top-3 global CRO with significant clinical technology and decentralized trial capabilities following its PRA Health Sciences acquisition. It directly competes with MedAvante for endpoint and eCOA work within full-service CRO engagements.
- Medpace: Medpace is a full-service CRO focused on small-to-mid biotech, with growing clinical technology capabilities. It competes with MedAvante for endpoint work, particularly from emerging biotech sponsors.
- Oracle Health Sciences (Clinical One / Inform): Oracle's Health Sciences unit (inheriting Phase Forward and Covance assets) offers EDC, CTMS, and eClinical platforms. It competes with MedAvante's trial enablement technology and is embedded in many large pharma technology stacks.
Emerging players
- Castor EDC: Castor is an emerging clinical trial data capture and eClinical platform competing in the same eCOA/EDC category as MedAvante's trial enablement offerings, particularly for smaller and academic-led studies.
- BioClin (now part of WCG) / WCG Clinical: WCG and its affiliates provide eCOA, rater training, and CNS clinical solutions (including the MedAvante-ProTrials heritage businesses). They overlap with MedAvante on rater-based outcome assessments and CNS trial enablement.
Market position
Strengths5 records
Weaknesses5 records
Competitive moat6 records
Key risks5 records
Key highlights7 records
Customer concentration
MedAvante social profiles
Digital presenceMedAvante financial estimates
Financial estimateRevenue estimate
Valuation estimate
MedAvante leadership team
Management profileNumber of profiles
Profiles7 records
MedAvante funding detail
Funding detailFunding overview
Funding rounds2 records
Investors2 records
Funding detail is available on the Subscription and Enterprise plan.Contact sales →
MedAvante M&A and investment
M&A and investmentM&A
Investments
M&A and investment is available on the Subscription and Enterprise plan.Contact sales →
Frequently asked questions about MedAvante
What does MedAvante do?
MedAvante provides technology-enabled clinical trial endpoint solutions for pharmaceutical, biotechnology, and CRO sponsors. Its offerings span electronic clinical outcome assessments (eCOA), cardiac safety monitoring, medical imaging core lab services, precision motion wearables (Opal System), respiratory function testing, and cloud-native trial enablement software. These solutions are delivered across site-based, hybrid, and decentralized clinical trial models in over 100 countries.
Is MedAvante a public or private company?
MedAvante is a private company. It is classified as corporate owned and is currently operating.
When was MedAvante founded?
MedAvante was founded in 2002. It employs 101 to 250 people.
Where is MedAvante based?
MedAvante is headquartered in Hackensack, United States, in the North America region.
Who are MedAvante's main competitors?
Direct peers on record are Veeva Systems and Signant Health. Broad incumbents are Parexel, IQVIA, Labcorp Drug Development (Fortrea), ICON plc, Medpace and Oracle Health Sciences (Clinical One / Inform). Emerging players are Castor EDC and BioClin (now part of WCG) / WCG Clinical.
Does MedAvante have an API?
No public API is recorded for MedAvante.
What industry is MedAvante in?
MedAvante's product category is Clinical Trial Endpoint Technology. Its primary akta.pro industry code is HLACAOAB, eCOA/ePRO/eDiary & Patient-Facing Data Collection, with a secondary code of HLAGAJAM, Clinical Trial Informatics (EDC/CTMS/eCOA/eTMF). Its NAICS code is 541690 and its SIC code is 7372.