Developer docs
API playgroundTry for free, no card

Search company profiles

Advarra

Full company profile

uuid00037fp

Namestring
Advarra
Legal namestring
Advarra, Inc.
Websiteurl
advarra.com
Company typeenum
Private
Founded yearint
1993
Descriptiontext

Advarra is a Columbia, Maryland-based clinical research technology company serving sponsors, CROs, academic medical centers, and investigator sites across the drug development lifecycle. Founded in 1993 and operating with 501-1,000 employees, it provides AAHRPP-accredited central IRB review services (CIRBI), enterprise CTMS platforms (OnCore for academic medical centers, Clinical Conductor for sites), an investigator community covering 50,000+ investigators, complementary offerings in IBC review, eSource, eRegulatory, DMC oversight, and GxP services, plus the Study Collaboration protocol site-portal product (formerly Longboat). The company reports 3,500+ institutions on its networks, 12,000+ open protocols annually, 3M+ patient visits, and $4B+ in trial invoice value flowing through its systems, with claimed penetration of 88% of NCI-designated cancer centers and 100% of top-10 pharma sponsors and CROs for IRB services.

Revenue mechanics combine multi-year subscription licenses for CTMS and Study Collaboration, per-protocol IRB and IBC review fees, ancillary compliance services, and enterprise contracts with major sponsors and CROs. Recent commercial activity in 2025-2026 — including the launch of the Braid AI and analytics platform and an AI-powered Study Design product, the appointment of a CTO, the addition of five eClinical partner integrations, an EHR-to-EDC interoperability partnership with IgniteData, and a site-network partnership with ICON plc — points to an explicit strategy to extend Advarra from review and workflow systems into an AI-enabled data and protocol design layer for the broader clinical research stack.

Short descriptiontext

Advarra is a Columbia, Maryland-based clinical research technology company providing central IRB review, enterprise CTMS (OnCore, Clinical Conductor), and the Study Collaboration site platform for pharma sponsors, CROs, and 3,500+ academic and research institutions worldwide.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
501–1,000
akta.pro rankint
HeadquartersColumbia, United States
HQ citystring
Columbia
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
clinical trial management, IRB review services, clinical research software, eClinical platform, institutional review board
Industry3 codes
1Clinical CROs (Phase I–IV)
CodeHLAGAAAAPrimaryYes
2Patient Recruitment, Site Feasibility & Trial Enablement CROs
CodeHLAGAAAIPrimaryNo
3Electronic Data Capture (EDC) Platforms
CodeHLACAOAAPrimaryNo
NAICS code1 code
  • Custom Computer Programming Services541511
SIC code2 codes
  • Services-Prepackaged Software7372
  • Services-Computer Programming Services7371
Product category
Clinical Trial Management Software
Social media profiles2 records
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model5 records
1CTMS Platform Subscriptions
TypeSubscription Recurring
Description

Annual or multi-year subscription licensing for OnCore and Clinical Conductor CTMS platforms, typically sold as enterprise agreements to research sites, academic medical centers, and health systems.

advarra.com
2Study Collaboration Platform
TypeSubscription Recurring
Description

Subscription-based access to connected site network and eClinical integrations for sponsors and CROs, with per-seat or site-based licensing models.

advarra.com
3IRB Review Services
TypeSubscription Recurring
Description

Regulatory review services for clinical trials, providing independent oversight with speed and transparency. Revenue from review fees and service agreements.

advarra.com
4AI and Data Platform (Braid)
TypeSubscription Recurring
Description

AI-powered insights and operational intelligence services, likely bundled with platform subscriptions or offered as add-on capabilities.

advarra.com
5Professional Services
TypeProfessional Services
Description

Consulting and professional services including study startup, coverage analysis, budget negotiation, and CTMS configuration services.

markets.financialcontent.com
Marketing channels9 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels4 records

Each record includes

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

Cost components5 values
Personnel, Technology or R&D, Operations, Marketing or Sales, Infrastructure
GTM typeB2B
B2B
Offering typeSoftware
Software
Brand1 of 9 records shown
1CIRBI
Description

IRB platform for managing institutional review board submissions and reviews

advarra.com
+8 more records
Core offering1 text field

Advarra provides clinical research technology and regulatory oversight products, including IRB review services through its CIRBI platform, enterprise CTMS solutions (OnCore and Clinical Conductor), eSource and eRegulatory document systems for research sites, and a Study Collaboration platform that connects sponsors, CROs, and sites via single sign-on to integrated eClinical technologies. Its Braid AI and data engine adds operational intelligence across the protocol lifecycle.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 7 values shown
  • 88% of NCI-designated cancer centers use Advarra technology
+6 more records
Product overview1 text field

Advarra is a clinical research technology platform combining IRB oversight, operational intelligence, and collaborative trial management. The core offerings include CIRBI for IRB services and the Braid AI and data engine platform. For research sites, Advarra provides OnCore (enterprise CTMS for academic medical centers and cancer centers) and Clinical Conductor (CTMS for sites, networks, and health systems), along with eReg (regulatory document management) and eSource (electronic data capture). For sponsors and CROs, the Study Collaboration platform integrates AI-powered Study Design, Site Identification & Feasibility, Study Startup, Site Collaboration & Training, and Enrollment Planning & Tracking. Additional offerings include IBC, DMC, and GxP compliance services. The Braid platform weaves operational intelligence from Advarra's IRB and clinical trial systems throughout the entire protocol lifecycle.

Product and service10 records
1CIRBI (Center for IRB Intelligence)
CategoryIRB review services
Description

Advarra's IRB platform providing independent, rigorous oversight with speed, expertise and transparency for ethical review of clinical research protocols, used by 100% of the top 10 pharmaceutical sponsors and CROs.

2Braid
CategoryAI and data platform
Description

Advarra's AI and data engine platform that weaves operational intelligence into the protocol lifecycle, powering Study Collaboration and providing actionable insights for smarter study design, faster decisions, and AI-automated workflows.

3OnCore
CategoryClinical Trial Management System (CTMS)
Description

Enterprise CTMS designed for academic medical centers and cancer centers, managing all operational aspects of clinical trials from study startup to closeout. Used by 88% of NCI-designated cancer centers.

4Clinical Conductor
CategoryClinical Trial Management System (CTMS)
Description

CTMS for research sites, site networks, hospitals, and health systems to manage research operations, study conduct, financial management, billing, and regulatory compliance.

5eReg
CategoryRegulatory document management
Description

Electronic regulatory document management and exchange system for efficient regulatory compliance at research sites.

6eSource
CategoryElectronic source data capture
Description

Integrated data capture and oversight system enabling electronic source documentation for clinical trials.

7Study Collaboration (formerly Longboat)
CategoryConnected site network platform
Description

Study collaboration solution providing sponsors, CROs, and research sites a single access point for clinical trial systems with single sign-on, credential management, and integrated eClinical technology partners.

8IBC (Institutional Biosafety Committee) Services
CategoryBiosafety review services
Description

Review and audit services for institutional biosafety committee oversight of gene therapy, cell therapy, and biologics research.

9DMC (Data Monitoring Committee) Services
CategoryData monitoring committee services
Description

Data monitoring committee services providing independent oversight of clinical trial safety data.

10GxP Compliance Intelligence
CategoryCompliance services
Description

Compliance intelligence services for GxP regulatory requirements in clinical research.

Scale indicator8 records

Each record includes

Type, Value, Description, Source

Partnership7 partners
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-03-24
Description

Definitive partnership to introduce a 'research-ready' connected site network model for clinical trials globally. Integration of ICON's global clinical trial solutions with Advarra's site CTMSs, eISF, and eSource systems used by 50,000+ investigators. Aims to reduce administrative friction, accelerate study startup, and increase clinical trial participation.

Strategic tierSecondaryTypeTechnology or IntegrationAnnounced on2025-12-10
Description

eClinical technology partner integrated into Advarra's Study Collaboration solution. YPrime provides clinical trial technology solutions and is part of the expanded partner network providing single sign-on access through Advarra's platform.

Strategic tierSecondaryTypeTechnology or IntegrationAnnounced on2025-12-10
Description

eClinical technology partner integrated into Advarra's Study Collaboration solution. Scout's technology is accessible through single sign-on within Advarra's platform ecosystem.

Strategic tierSecondaryTypeTechnology or IntegrationAnnounced on2025-12-10
Description

eClinical technology partner integrated into Advarra's Study Collaboration solution. Suvoda's solutions are accessible through single sign-on within Advarra's platform.

Strategic tierSecondaryTypeTechnology or IntegrationAnnounced on2025-12-10
Description

eClinical technology partner integrated into Advarra's Study Collaboration solution. Datacubed's technology is accessible through single sign-on within Advarra's platform.

Strategic tierSecondaryTypeTechnology or IntegrationAnnounced on2025-12-10
Description

eClinical technology partner integrated into Advarra's Study Collaboration solution. Endpoint's technology is accessible through single sign-on within Advarra's platform.

Strategic tierCoreTypeTechnology or IntegrationAnnounced on2025-11-12
Description

Partnership to enhance clinical trial data transfer between research sites' EHR systems, Advarra's eSource and EDC systems, and sponsor EDC systems. Collaboration aims to improve data accuracy, reduce administrative burden, and accelerate clinical trial conduct.

Recent move8 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Veeva provides CTMS, eTMF, Vault Clinical, and a broad clinical operations suite for pharma sponsors and CROs, competing directly with Advarra's Study Collaboration and CTMS offerings for sponsor-side wallet share.

TypeDirect peer
Description

Medidata's Rave EDC, CTMS, eCOA, and RTSM platform competes with Advarra's eSource, Clinical Conductor, and integrated eClinical partners across sponsor and CRO customers.

TypeDirect peer
Description

WCG is Advarra's most direct IRB services competitor, providing independent review boards and clinical services to sponsors, CROs, and research sites across all therapeutic areas.

TypeBroad incumbent
Description

Oracle's Clinical One platform unifies EDC, RTSM, CTMS, and ePRO, competing with Advarra's integrated eClinical vision for large enterprise pharma customers.

TypeBroad incumbent
Description

IQVIA combines CRO services with proprietary clinical trial technology (e.g., IQVIA Technologies, Digital Trial Solutions), positioning as a broader incumbent that overlaps with Advarra's sponsor-side offerings.

TypeDirect peer
Description

Clario provides eCOA, cardiac safety, respiratory, and imaging solutions integrated into clinical trials, directly competing with Advarra's eClinical partner ecosystem for sponsor eClinical spend.

TypeDirect peer
Description

Signant Health offers eCOA, eConsent, RTSM, patient engagement, and clinical supply technology, overlapping with Advarra's Study Collaboration partner integrations and eSource offerings.

TypeEmerging player
Description

Florence provides eISF and site-focused clinical trial technology that directly competes with Advarra's eReg, eISF, and site CTMS offerings for academic and community research sites.

TypeEmerging player
Description

Castor offers an EDC and eClinical platform with strong adoption among academic medical centers and emerging sponsors, competing with Advarra's Clinical Conductor and eSource offerings in the site segment.

TypeOthers
Description

ICON is both Advarra's strategic partner (connected site network) and a global CRO with proprietary technology. As a distribution partner, ICON extends Advarra's reach; as a CRO with competing site technology, it represents a complex peer relationship.

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 customers8 records

Each record includes

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

Segment3 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
Yes

Docs URL, Description

Integration13 records

Each record includes

Title, Type, Description, Source

AI capability6 records

Each record includes

Type, Description, Source

AI maturity
App detail

Has app

Feature8 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles9 records

Each record includes

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

No data
Compliance7 records

Each record includes

Name, Class, Description

Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds

Each record includes

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

Investors

Each record includes

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

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

M&A6 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 →

Advarra

Clinical Trial Management Softwareadvarra.com

Advarra is a Columbia, Maryland-based clinical research technology company providing central IRB review, enterprise CTMS (OnCore, Clinical Conductor), and the Study Collaboration site platform for pharma sponsors, CROs, and 3,500+ academic and research institutions worldwide.

What Advarra does

Advarra is a Columbia, Maryland-based clinical research technology company serving sponsors, CROs, academic medical centers, and investigator sites across the drug development lifecycle. Founded in 1993 and operating with 501-1,000 employees, it provides AAHRPP-accredited central IRB review services (CIRBI), enterprise CTMS platforms (OnCore for academic medical centers, Clinical Conductor for sites), an investigator community covering 50,000+ investigators, complementary offerings in IBC review, eSource, eRegulatory, DMC oversight, and GxP services, plus the Study Collaboration protocol site-portal product (formerly Longboat). The company reports 3,500+ institutions on its networks, 12,000+ open protocols annually, 3M+ patient visits, and $4B+ in trial invoice value flowing through its systems, with claimed penetration of 88% of NCI-designated cancer centers and 100% of top-10 pharma sponsors and CROs for IRB services.

Revenue mechanics combine multi-year subscription licenses for CTMS and Study Collaboration, per-protocol IRB and IBC review fees, ancillary compliance services, and enterprise contracts with major sponsors and CROs. Recent commercial activity in 2025-2026 — including the launch of the Braid AI and analytics platform and an AI-powered Study Design product, the appointment of a CTO, the addition of five eClinical partner integrations, an EHR-to-EDC interoperability partnership with IgniteData, and a site-network partnership with ICON plc — points to an explicit strategy to extend Advarra from review and workflow systems into an AI-enabled data and protocol design layer for the broader clinical research stack.

Advarra firmographics

Firmographics
Name
Advarra
Legal name
Advarra, Inc.
Website
https://advarra.com
Company type
Private
Founded year
1993
Operating status
Operating
Headcount range
501–1,000 employees
Short description
Advarra is a Columbia, Maryland-based clinical research technology company providing central IRB review, enterprise CTMS (OnCore, Clinical Conductor), and the Study Collaboration site platform for pharma sponsors, CROs, and 3,500+ academic and research institutions worldwide.
Ownership category
akta.pro rank

Advarra industry classification

Industry
Product category
Clinical Trial Management Software
NAICS
Custom Computer Programming Services (541511)
SIC
Services-Prepackaged Software (7372), Services-Computer Programming Services (7371)
akta.pro primary industry
Clinical CROs (Phase I–IV) (HLAGAAAA)
akta.pro secondary industries
Patient Recruitment, Site Feasibility & Trial Enablement CROs (HLAGAAAI), Electronic Data Capture (EDC) Platforms (HLACAOAA)

Keywords

  • Clinical trial management
  • IRB review services
  • Clinical research software
  • EClinical platform
  • Institutional review board

Where Advarra is headquartered

Location

Headquarters

HQ city
Columbia
HQ country
United States
HQ region
North America

Offices1 record

Markets served

Advarra business model

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

Revenue model

  1. CTMS Platform Subscriptions: Annual or multi-year subscription licensing for OnCore and Clinical Conductor CTMS platforms, typically sold as enterprise agreements to research sites, academic medical centers, and health systems.
  2. Study Collaboration Platform: Subscription-based access to connected site network and eClinical integrations for sponsors and CROs, with per-seat or site-based licensing models.
  3. IRB Review Services: Regulatory review services for clinical trials, providing independent oversight with speed and transparency. Revenue from review fees and service agreements.
  4. AI and Data Platform (Braid): AI-powered insights and operational intelligence services, likely bundled with platform subscriptions or offered as add-on capabilities.
  5. Professional Services: Consulting and professional services including study startup, coverage analysis, budget negotiation, and CTMS configuration services.

Go-to-market motion2 records

Distribution channels4 records

Marketing channels9 records

Advarra product offering

Product offering

Core offering

Advarra provides clinical research technology and regulatory oversight products, including IRB review services through its CIRBI platform, enterprise CTMS solutions (OnCore and Clinical Conductor), eSource and eRegulatory document systems for research sites, and a Study Collaboration platform that connects sponsors, CROs, and sites via single sign-on to integrated eClinical technologies. Its Braid AI and data engine adds operational intelligence across the protocol lifecycle.

Product overview

Advarra is a clinical research technology platform combining IRB oversight, operational intelligence, and collaborative trial management. The core offerings include CIRBI for IRB services and the Braid AI and data engine platform. For research sites, Advarra provides OnCore (enterprise CTMS for academic medical centers and cancer centers) and Clinical Conductor (CTMS for sites, networks, and health systems), along with eReg (regulatory document management) and eSource (electronic data capture). For sponsors and CROs, the Study Collaboration platform integrates AI-powered Study Design, Site Identification & Feasibility, Study Startup, Site Collaboration & Training, and Enrollment Planning & Tracking. Additional offerings include IBC, DMC, and GxP compliance services. The Braid platform weaves operational intelligence from Advarra's IRB and clinical trial systems throughout the entire protocol lifecycle.

Differentiator

Problem solved

Functional benefit

Brands

  • CIRBI: IRB platform for managing institutional review board submissions and reviews
  • OnCore
  • Clinical Conductor
  • Braid
  • Study Collaboration
  • eReg
  • eSource
  • IBC Services
  • DMC Services

Products and services

  • CIRBI (Center for IRB Intelligence) Advarra's IRB platform providing independent, rigorous oversight with speed, expertise and transparency for ethical review of clinical research protocols, used by 100% of the top 10 pharmaceutical sponsors and CROs.
  • Braid Advarra's AI and data engine platform that weaves operational intelligence into the protocol lifecycle, powering Study Collaboration and providing actionable insights for smarter study design, faster decisions, and AI-automated workflows.
  • OnCore Enterprise CTMS designed for academic medical centers and cancer centers, managing all operational aspects of clinical trials from study startup to closeout. Used by 88% of NCI-designated cancer centers.
  • Clinical Conductor CTMS for research sites, site networks, hospitals, and health systems to manage research operations, study conduct, financial management, billing, and regulatory compliance.
  • eReg Electronic regulatory document management and exchange system for efficient regulatory compliance at research sites.
  • eSource Integrated data capture and oversight system enabling electronic source documentation for clinical trials.
  • Study Collaboration (formerly Longboat) Study collaboration solution providing sponsors, CROs, and research sites a single access point for clinical trial systems with single sign-on, credential management, and integrated eClinical technology partners.
  • IBC (Institutional Biosafety Committee) Services Review and audit services for institutional biosafety committee oversight of gene therapy, cell therapy, and biologics research.
  • DMC (Data Monitoring Committee) Services Data monitoring committee services providing independent oversight of clinical trial safety data.
  • GxP Compliance Intelligence Compliance intelligence services for GxP regulatory requirements in clinical research.

Quantifiable outcome

  • 88% of NCI-designated cancer centers use Advarra technology
  • +6 more outcomes

Companies that use Advarra

Customer profile

Named customers8 records

Segments3 records

Ideal customer profiles3 records

Advarra technology and API

Technology

Technology focussed Yes

API detail

Has API
Yes
API docs
API detail

Core technology

AI maturity

App detail

Integration13 records

AI capability6 records

Feature8 records

Advarra partnerships and signals

Strategic signal

Partnerships

Seven partnerships are on record, tiered core and secondary.

  • ICON plccoreStrategic or Co-development Partner · 24 March 2026Definitive partnership to introduce a 'research-ready' connected site network model for clinical trials globally. Integration of ICON's global clinical trial solutions with Advarra's site CTMSs, eISF, and eSource systems used by 50,000+ investigators. Aims to reduce administrative friction, accelerate study startup, and increase clinical trial participation.
  • YPrimesecondaryTechnology or Integration · 10 December 2025eClinical technology partner integrated into Advarra's Study Collaboration solution. YPrime provides clinical trial technology solutions and is part of the expanded partner network providing single sign-on access through Advarra's platform.
  • ScoutsecondaryTechnology or Integration · 10 December 2025eClinical technology partner integrated into Advarra's Study Collaboration solution. Scout's technology is accessible through single sign-on within Advarra's platform ecosystem.
  • SuvodasecondaryTechnology or Integration · 10 December 2025eClinical technology partner integrated into Advarra's Study Collaboration solution. Suvoda's solutions are accessible through single sign-on within Advarra's platform.
  • DatacubedsecondaryTechnology or Integration · 10 December 2025eClinical technology partner integrated into Advarra's Study Collaboration solution. Datacubed's technology is accessible through single sign-on within Advarra's platform.
  • EndpointsecondaryTechnology or Integration · 10 December 2025eClinical technology partner integrated into Advarra's Study Collaboration solution. Endpoint's technology is accessible through single sign-on within Advarra's platform.
  • IgniteDatacoreTechnology or Integration · 12 November 2025Partnership to enhance clinical trial data transfer between research sites' EHR systems, Advarra's eSource and EDC systems, and sponsor EDC systems. Collaboration aims to improve data accuracy, reduce administrative burden, and accelerate clinical trial conduct.

Scale indicators8 records

Recent moves8 records

Expansion highlights5 records

Advarra competitors and assessment

Company assessment

Direct peers

  • Veeva Systems: Veeva provides CTMS, eTMF, Vault Clinical, and a broad clinical operations suite for pharma sponsors and CROs, competing directly with Advarra's Study Collaboration and CTMS offerings for sponsor-side wallet share.
  • Medidata (Dassault Systèmes): Medidata's Rave EDC, CTMS, eCOA, and RTSM platform competes with Advarra's eSource, Clinical Conductor, and integrated eClinical partners across sponsor and CRO customers.
  • WCG (WIRB-Copernicus Group): WCG is Advarra's most direct IRB services competitor, providing independent review boards and clinical services to sponsors, CROs, and research sites across all therapeutic areas.
  • Clario (formerly ERT): Clario provides eCOA, cardiac safety, respiratory, and imaging solutions integrated into clinical trials, directly competing with Advarra's eClinical partner ecosystem for sponsor eClinical spend.
  • Signant Health: Signant Health offers eCOA, eConsent, RTSM, patient engagement, and clinical supply technology, overlapping with Advarra's Study Collaboration partner integrations and eSource offerings.

Broad incumbents

  • Oracle Health Sciences (Clinical One): Oracle's Clinical One platform unifies EDC, RTSM, CTMS, and ePRO, competing with Advarra's integrated eClinical vision for large enterprise pharma customers.
  • IQVIA Technologies: IQVIA combines CRO services with proprietary clinical trial technology (e.g., IQVIA Technologies, Digital Trial Solutions), positioning as a broader incumbent that overlaps with Advarra's sponsor-side offerings.

Emerging players

  • Florence Healthcare: Florence provides eISF and site-focused clinical trial technology that directly competes with Advarra's eReg, eISF, and site CTMS offerings for academic and community research sites.
  • Castor: Castor offers an EDC and eClinical platform with strong adoption among academic medical centers and emerging sponsors, competing with Advarra's Clinical Conductor and eSource offerings in the site segment.

Others

  • ICON plc: ICON is both Advarra's strategic partner (connected site network) and a global CRO with proprietary technology. As a distribution partner, ICON extends Advarra's reach; as a CRO with competing site technology, it represents a complex peer relationship.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat6 records

Key risks6 records

Key highlights7 records

Customer concentration

Advarra social profiles

Digital presence

Advarra compliance and trust

Trust signal

Compliance7 records

Advarra financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Advarra leadership team

Management profile

Number of profiles

Profiles9 records

Advarra funding detail

Funding detail

Funding overview

Funding rounds

Investors

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

Advarra M&A and investment

M&A and investment

M&A6 records

Investments

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

Frequently asked questions about Advarra

What does Advarra do?

Advarra provides clinical research technology and regulatory oversight products, including IRB review services through its CIRBI platform, enterprise CTMS solutions (OnCore and Clinical Conductor), eSource and eRegulatory document systems for research sites, and a Study Collaboration platform that connects sponsors, CROs, and sites via single sign-on to integrated eClinical technologies. Its Braid AI and data engine adds operational intelligence across the protocol lifecycle.

Is Advarra a public or private company?

Advarra is a private company. It is classified as unknown and is currently operating.

When was Advarra founded?

Advarra was founded in 1993. It employs 501 to 1,000 people.

Where is Advarra based?

Advarra is headquartered in Columbia, United States, in the North America region.

How does Advarra make money?

Five revenue lines are on record. CTMS Platform Subscriptions are the primary driver. The others are study Collaboration Platform, IRB Review Services, AI and Data Platform (Braid) and professional Services.

Who are Advarra's main competitors?

Direct peers on record are Veeva Systems, Medidata (Dassault Systèmes), WCG (WIRB-Copernicus Group), Clario (formerly ERT) and Signant Health. Broad incumbents are Oracle Health Sciences (Clinical One) and IQVIA Technologies. Emerging players are Florence Healthcare and Castor. ICON plc is listed as an others.

Does Advarra have an API?

Yes. Advarra provides a Study Collaboration platform that connects sponsors, CROs, and research sites with integrated eClinical technologies. The platform offers single sign-on (SSO) access to multiple systems including EDC, eConsent, IRT/RTSM, eCOA, payments, and patient engagement tools. The platform is used by more than 225,000 study team members. The CTMS integrations support API connections for linking with various enterprise systems including eRegulatory, eIRB, EDC, and participant payments.

What industry is Advarra in?

Advarra's product category is Clinical Trial Management Software. Its primary akta.pro industry code is HLAGAAAA, Clinical CROs (Phase I–IV), with a secondary code of HLAGAAAI, Patient Recruitment, Site Feasibility & Trial Enablement CROs. Its NAICS code is 541511 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 NewswireAdvarra Launches Site Identification Technology with Insights Directly from SitesAdvarra launched Site ID technology, combining eIRB-validated insights with clinical trial management system data to help sponsors and CROs identify high-performing research sites. The solution aims to reduce site selection uncertainty, citing that site activation takes seven months and delays can cost over $25,000. It is available via a self-service app and a service with no software commitment.Quiver QuantitativeMedicus Pharma Receives FDA Feedback and Central IRB Approval for Optimized Phase 2 Teverelix Study in Acute Urinary Retention | Quiver QuantitativeMedicus Pharma Ltd. announced receiving written FDA feedback and central IRB (Advarra) approval for its optimized Phase 2 clinical study of Teverelix in men following acute urinary retention. The redesigned study ANT-2111-02 will enroll approximately 126 patients across the United States and Europe, significantly reduced from the previously planned 390 patients. The FDA provided seven operational recommendations regarding protocol implementation and safety monitoring, which the company believes do not require changes to the study's scientific rationale, primary endpoint, or treatment arms.Stock TitanMedicus Pharma FDA Feedback on 126-Patient Teverelix StudyMedicus Pharma Ltd. announced it received positive written feedback from the U.S. Food and Drug Administration and central Institutional Review Board approval for its optimized Phase 2 clinical study of Teverelix® in men following acute urinary retention. The FDA provided its written response on July 8, 2026, with seven operational comments regarding protocol implementation, safety monitoring, and clarity, while Advarra approved the protocol on June 18, 2026. The redesigned study is expected to enroll approximately 126 patients across the United States and Europe, compared with approximately 390 patients under the previously disclosed development plan, representing a two-thirds reduction in enrollment while preserving the ability to generate decision-grade clinical evidence.EIN PresswireThe Top Clinical Trial Management Software According to the FeaturedCustomers Summer 2026 Customer Success ReportFeaturedCustomers released its Summer 2026 Clinical Trial Management Software Customer Success Report, ranking vendors by customer reference content. Market Leaders include Advarra, ArisGlobal, IQVIA, Medidata, and Veeva; Top Performers include Castor EDC, CRIO, and others; Rising Stars include CliniOps, Crucial Data Solutions, and Ennov. The report is based on over 2,000 verified customer references.openPR.comInstitutional Review Board Irb Systems Market Is Going to Boom | • Advarra • Quorum Review IRB • WCG IRBA market research report has been released indicating that the Institutional Review Board (IRB) systems market is expected to grow significantly through 2026-2033. The report covers industry trends, major players, regional performance, and growth prospects, highlighting the importance of technological innovation and sustainability.Simply Wall StWhy ICON (ICLR) Is Up 5.1% After New AI-Powered Clinical Trial Partnership With AdvarraIn March 2026, Advarra announced a definitive partnership with ICON plc to create a 'research-ready' connected site network integrating ICON's clinical trial solutions with Advarra's site CTMS, eISF, and eSource systems used by over 50,000 investigators globally. Advarra's AI and data platform will supply ICON with operational intelligence to improve protocol design, planning, and site selection, potentially reducing trial cancellations and delays that have weighed on near-term revenue visibility. The article situates this partnership within ICON's broader AI strategy, including tools like iSubmit and AI-enabled forecasting, as part of an effort to compress study cycle times in a competitive CRO market facing pricing pressure.FierceBiotechIcon, Advarra partnership aims to optimize trials, expand accessClinical research organization Icon has partnered with research technology company Advarra to launch a network of connected sites for clinical trials, combining Icon's global clinical trial solutions with Advarra's systems used by 50,000 investigators worldwide. The collaboration will allow Icon's proprietary technology to operate within a shared environment, with Advarra providing AI platform access to improve protocol design, forecasting, and study planning. The companies also aim to expand clinical trial access in emerging markets by standardizing operations and reducing manual work.Stock TitanICON, Advarra link trial tech for site networkICON plc and Advarra have entered a definitive partnership to introduce a new 'research-ready,' connected site network model for clinical trials. The partnership will integrate ICON's global clinical trial solutions with Advarra's site CTMSs, eISF, and eSource systems, which are already used by more than 50,000 investigators worldwide. The collaboration aims to reduce administrative friction, accelerate study startup, expand access to clinical trials, and help more research sites support increasingly complex study requirements.PharmiWeb.comICON and Advarra launch connected site network modelICON and Advarra have partnered to develop a connected site network model to facilitate clinical trials by linking ICON’s technology with Advarra’s existing systems. The initiative aims to reduce administrative burdens, enhance study startup, and increase participation in complex trials.FinancialContent Business PageICON and Advarra Introduce New ‘Research-Ready,’ Connected Site Network ModelICON plc and Advarra have entered into a definitive partnership to introduce a new 'research-ready,' connected site network model for clinical trials, integrating ICON's clinical trial solutions with Advarra's site technology systems. The partnership will leverage Advarra's Study Collaboration platform built on its data and AI platform to create a shared operating environment that reduces administrative friction, accelerates study startup, and increases clinical trial participation. Advarra's site systems currently manage over $4 billion in trial invoice value, over 3 million patient visits, and are used by more than 50,000 investigators worldwide.