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BioClinica

Full company profile

uuid003fe2b

Namestring
BioClinica
Websiteurl
bioclinica.com
Company typeenum
Private
Founded yearint
1998
Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
1,001–5,000
akta.pro rankint
HeadquartersNewtown, United States
HQ citystring
Newtown
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Keyword5 values
clinical trial management, pharmacovigilance solutions, medical imaging trials, eCOA clinical trials, cardiac safety assessment
Industry3 codes
1Biosimilar Development & Clinical/Regulatory Services (comparability, trials, pharmacovigilance)
CodeHLAAAHAJPrimaryNo
2Post-Approval Clinical Development (Phase IV & Lifecycle Management)
CodeHLAIALAJPrimaryNo
3Biostatistics, Statistical Computing & Clinical Programming (SAS/R/Pipelines)
CodeHLACAOAOPrimaryNo
NAICS code1 code
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
SIC code1 code
  • Services-Commercial Physical & Biological Research8731
Product category
Clinical Trial Management Software
Social media profiles3 records
Cost components4 values
Personnel, Technology or R&D, Operations, Marketing or Sales
GTM typeB2B
B2B
Offering typeSoftware
Software
Core offering1 text field

BioClinica provides integrated, technology-enhanced clinical trial management solutions for the pharmaceutical and biotechnology industries. The company is positioned as a key technology and services provider in the pharmacovigilance market, supporting drug safety and adverse event monitoring across clinical development programs.

Differentiator
Functional benefit
Problem solved
Product and service1 record
1Pharmacovigilance Solutions
Scale indicator1 record

Each record includes

Type, Value, Description, Source

Expansion highlight4 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Veeva's Vault Clinical and Vault Safety suites compete directly with BioClinica's EDC, CTMS, and pharmacovigilance technology offerings. Veeva is a key benchmark for cloud-native clinical and safety platforms targeting the same sponsor buyers.

TypeDirect peer
Description

ArisGlobal provides LifeSphere Safety and other pharmacovigilance and regulatory platforms, and is explicitly named alongside BioClinica in the Germany PV market. It is a direct competitor in the same PV technology and services category.

TypeBroad incumbent
Description

ICON is a top-3 global CRO with deep clinical operations and a technology platform (including Firecrest and ICONIK). It competes with BioClinica for full-service and embedded technology-enabled trial management engagements across pharma and biotech.

TypeBroad incumbent
Description

Parexel is a global CRO with biopharmaceutical services, clinical trial technology, and pharmacovigilance capabilities. It competes with BioClinica for both functional service and full-service clinical trial engagements.

TypeBroad incumbent
Description

IQVIA is the largest global CRO with embedded technology (E360, Orchestrated Patient Engagement) and a sizable pharmacovigilance practice. It overlaps BioClinica's clinical operations, technology-enabled trial management, and PV offerings, but at substantially greater scale and broader service breadth.

TypeBroad incumbent
Description

Fortrea provides clinical development and safety/PV services carved out from Labcorp. It is a direct competitor to BioClinica across early- and late-phase clinical operations and post-market pharmacovigilance.

TypeDirect peer
Description

Clario was formed from the combination of BioClinica and ERT and offers clinical trial endpoint technology, imaging, eCOA, and PV services. It is the most directly comparable peer because BioClinica's clinical trial management and imaging core lab capabilities map one-to-one onto Clario's portfolio today.

TypeDirect peer
Description

Signant Health specializes in eCOA, eConsent, patient engagement, and clinical trial technology, overlapping BioClinica's technology-enabled trial management solutions (notably via Blueprint Clinical heritage). It is a focused technology peer rather than a broad CRO.

TypeDirect peer
Description

Medidata provides the Rave EDC, eCOA, imaging, and RTSM platform that powers a large share of industry clinical trials. It is the principal technology-side competitor to BioClinica's clinical trial management solutions and is increasingly bundled with CRO services.

TypeBroad incumbent
Description

Oracle offers Clinical One RTSM/EDC, eClinical technology, and safety/PV solutions that overlap BioClinica's clinical trial management and pharmacovigilance offerings, typically sold into larger sponsor accounts with embedded Oracle footprints.

Market position
Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat4 records

Each record includes

Type, Details

Key highlights5 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Ideal customer profile1 record

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

AI maturity
App detail

Has app

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles2 records

Each record includes

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

No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds3 records

Each record includes

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

Investors1 record

Each record includes

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

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

M&A11 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 →

BioClinica

Clinical Trial Management Softwarebioclinica.com

BioClinica firmographics

Firmographics
Name
BioClinica
Website
https://bioclinica.com
Company type
Private
Founded year
1998
Operating status
Operating
Headcount range
1,001–5,000 employees
Ownership category
akta.pro rank

Where BioClinica is headquartered

Location

Headquarters

HQ city
Newtown
HQ country
United States
HQ region
North America

Markets served

BioClinica business model

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

BioClinica product offering

Product offering

Core offering

BioClinica provides integrated, technology-enhanced clinical trial management solutions for the pharmaceutical and biotechnology industries. The company is positioned as a key technology and services provider in the pharmacovigilance market, supporting drug safety and adverse event monitoring across clinical development programs.

Differentiator

Problem solved

Functional benefit

Products and services

  • Pharmacovigilance Solutions

Companies that use BioClinica

Customer profile

Ideal customer profiles1 record

BioClinica technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

BioClinica partnerships and signals

Strategic signal

Scale indicators1 record

Expansion highlights4 records

BioClinica competitors and assessment

Company assessment

Direct peers

  • Veeva Systems: Veeva's Vault Clinical and Vault Safety suites compete directly with BioClinica's EDC, CTMS, and pharmacovigilance technology offerings. Veeva is a key benchmark for cloud-native clinical and safety platforms targeting the same sponsor buyers.
  • ArisGlobal: ArisGlobal provides LifeSphere Safety and other pharmacovigilance and regulatory platforms, and is explicitly named alongside BioClinica in the Germany PV market. It is a direct competitor in the same PV technology and services category.
  • Clario: Clario was formed from the combination of BioClinica and ERT and offers clinical trial endpoint technology, imaging, eCOA, and PV services. It is the most directly comparable peer because BioClinica's clinical trial management and imaging core lab capabilities map one-to-one onto Clario's portfolio today.
  • Signant Health: Signant Health specializes in eCOA, eConsent, patient engagement, and clinical trial technology, overlapping BioClinica's technology-enabled trial management solutions (notably via Blueprint Clinical heritage). It is a focused technology peer rather than a broad CRO.
  • Medidata (Dassault Systèmes): Medidata provides the Rave EDC, eCOA, imaging, and RTSM platform that powers a large share of industry clinical trials. It is the principal technology-side competitor to BioClinica's clinical trial management solutions and is increasingly bundled with CRO services.

Broad incumbents

  • ICON plc: ICON is a top-3 global CRO with deep clinical operations and a technology platform (including Firecrest and ICONIK). It competes with BioClinica for full-service and embedded technology-enabled trial management engagements across pharma and biotech.
  • Parexel International: Parexel is a global CRO with biopharmaceutical services, clinical trial technology, and pharmacovigilance capabilities. It competes with BioClinica for both functional service and full-service clinical trial engagements.
  • IQVIA: IQVIA is the largest global CRO with embedded technology (E360, Orchestrated Patient Engagement) and a sizable pharmacovigilance practice. It overlaps BioClinica's clinical operations, technology-enabled trial management, and PV offerings, but at substantially greater scale and broader service breadth.
  • Fortrea (formerly Labcorp Drug Development): Fortrea provides clinical development and safety/PV services carved out from Labcorp. It is a direct competitor to BioClinica across early- and late-phase clinical operations and post-market pharmacovigilance.
  • Oracle Health Sciences (Clinical One / Siebel): Oracle offers Clinical One RTSM/EDC, eClinical technology, and safety/PV solutions that overlap BioClinica's clinical trial management and pharmacovigilance offerings, typically sold into larger sponsor accounts with embedded Oracle footprints.

Market position

Weaknesses5 records

Competitive moat4 records

Key highlights5 records

Customer concentration

BioClinica social profiles

Digital presence

BioClinica financial estimates

Financial estimate

Revenue estimate

Valuation estimate

BioClinica leadership team

Management profile

Number of profiles

Profiles2 records

BioClinica funding detail

Funding detail

Funding overview

Funding rounds3 records

Investors1 record

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

BioClinica M&A and investment

M&A and investment

M&A11 records

Investments

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

Frequently asked questions about BioClinica

What does BioClinica do?

BioClinica provides integrated, technology-enhanced clinical trial management solutions for the pharmaceutical and biotechnology industries. The company is positioned as a key technology and services provider in the pharmacovigilance market, supporting drug safety and adverse event monitoring across clinical development programs.

When was BioClinica founded?

BioClinica was founded in 1998. It employs 1,001 to 5,000 people.

Where is BioClinica based?

BioClinica is headquartered in Newtown, United States, in the North America region.

Who are BioClinica's main competitors?

Direct peers on record are Veeva Systems, ArisGlobal, Clario, Signant Health and Medidata (Dassault Systèmes). Broad incumbents are ICON plc, Parexel International, IQVIA, Fortrea (formerly Labcorp Drug Development) and Oracle Health Sciences (Clinical One / Siebel).

Does BioClinica have an API?

No public API is recorded for BioClinica.

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Live signals
openPR.comGermany Pharmacovigilance Market to grow at 12.43% CAGR | North America leads with 35% share | Top Companies - ArisGlobal, BioClinica, CognizantThe article reports that the Germany Pharmacovigilance Market is projected to grow at a CAGR of 12.43% from 2024 to 2031, supported by increased drug safety regulations and clinical trial volumes. Key companies providing technology and services in this market include ArisGlobal, BioClinica, and Cognizant.YahooAI-Powered Clinical Trial Management Market Forecasts Report 2024-2029, Profiles of Medidata, Oracle, IBM, Veeva Systems, Clinerion, Saama Technologies, Bioclinica, Arisglobal, Aicure, MedableThe AI-powered clinical trial management market is projected to grow from $1.794 billion in 2024 to $4.950 billion by 2029, a CAGR of 22.50%. Growth is driven by adoption by pharmaceutical companies and research institutions, with North America expected to see exponential growth.PR NewswireGlobal Clinical Trial Imaging Market Report 2021 to 2028 Featuring Market Players such as ICON, Bioclinica, Navitas Life Sciences, and Paraxel InternationalResearch and Markets published a global clinical trial imaging market report covering 2021-2028, projecting the market to reach USD 1.4 billion by 2028 at a compound annual growth rate of 6.1%. The growth is driven by increasing R&D spending for developing new drugs and therapies to treat chronic diseases, with clinical trial imaging being used across all phases of trials as a primary and quantitative biomarker. Market players such as ICON, Bioclinica, Navitas Life Sciences, and Paraxel International provide services including analytical testing, pharmacokinetic reading, and pharmacodynamics services for enhanced clinical development.PR NewswireERT Improves Patient Compliance in Cardiac Studies with Home Blood Pressure ServiceERT, a clinical endpoint data collection company, announced the expansion of its portfolio with an at-home blood pressure monitoring solution that completes its suite of BP assessment services for clinical trials. The solution aims to improve patient compliance and data collection frequency while reducing the "white coat effect" that can skew in-clinic readings. ERT also noted it is merging with Bioclinica to form a combined company with expanded industry expertise and market leadership in clinical-grade endpoint data collection.PR NewswireBioclinica Adds eConsent Functionality to Its Electronic Data Capture and Management Suite of ProductsBioclinica, an ERT company, announced the addition of eConsent to its Electronic Data Capture and Management product suite on June 8, 2021. The new electronic module supports the entire clinical trial consent process from IRB document approval through in-person or remote participant interactions, with deployment possible within eight weeks of protocol delivery. The company highlighted that the module helps sponsors and CROs reach diverse populations and improves participant understanding through multimedia components, knowledge reviews, and enhanced site-participant interactions.PR NewswireBioclinica Earns CRO Leadership Awards Fourth Consecutive YearBioclinica, an ERT company, announced it has received 2021 CRO Leadership Awards for the fourth consecutive year, recognized in the categories of Capabilities, Compatibility, Expertise, and Reliability. The awards are based on direct customer feedback surveyed by Industry Standard Research across 60 CROs evaluated in their annual quality benchmarking survey. Clinical Leader and Life Science Leader publications partnered with ISR to determine award recipients based on evaluations from pharma and biopharma decision-makers.PR NewswireERT e Bioclinica acertam fusão, criando a empresa líder global em tecnologia de endpoint de ensaios clínicosERT completed its merger with Bioclinica, creating a global leader in clinical trial endpoint technology and a leading partner for pharmaceutical and biotechnology companies. The transaction combines Bioclinica's expertise in imaging, software, eClinical, and drug safety solutions with ERT's expertise in eCOA, cardiac safety, respiratory, and wearables to form the most comprehensive endpoint data collection portfolio in the industry. The combined company, led by CEO Joe Eazor, is committed to accelerating R&D investments and delivering integrated digital solutions to improve clinical trial experiences for sites, clients, and patients.PR NewswireERT und Bioclinica schließen Fusion ab und schaffen den weltweit führenden Anbieter von Endpunkttechnologie für klinische StudienERT completed its merger with Bioclinica on April 28, 2021, creating the world's leading provider of endpoint technology for clinical trials. The transaction combines Bioclinica's expertise in clinical imaging, eClinical software, and drug safety solutions with ERT's capabilities in eCOA, cardiac safety, respiration, and wearables. Joe Eazor serves as President and CEO of the merged organization, which aims to accelerate R&D investments and provide more integrated endpoint technology to pharma and biotech companies.PR NewswireERT y Bioclinica se fusionan, creando el líder mundial en tecnología endpoint de ensayos clínicosERT announced the closing of its merger with Bioclinica on April 28, 2021, creating the world leader in clinical trial endpoint technology. The combined entity integrates Bioclinica's expertise in imaging, eClinical software, and drug safety solutions with ERT's capabilities in eCOA, cardiac safety, respiratory devices, and wearables. Joe Eazor, formerly CEO of ERT, leads the merged company, which commits to accelerating R&D investments to deliver more integrated endpoint technology to pharmaceutical and biotechnology clients.PR NewswireBioclinica Adds eTMF Functionality to CTMSBioclinica announced the addition of eTMF (electronic Trial Master File) functionality to its CTMS (Clinical Trial Management System) offering, leveraging an existing linked SharePoint environment to provide secure document storage for clinical trial tracking. The new module supports regulatory compliance with 21 CFR Part 11, offers full audit trails, version history, and role-based permissions while integrating with existing SharePoint workflow capabilities. Company executives described the addition as a transformational change that enables companies to use an integrated solution eliminating redundancies and improving workflows, with full operational capability achievable within weeks.