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MedAvante

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uuid000axcn

Namestring
MedAvante
Websiteurl
medavante.com
Company typeenum
Private
Founded yearint
2002
Descriptiontext

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.

Short descriptiontext

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.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
101–250
akta.pro rankint
HeadquartersHackensack, United States
HQ citystring
Hackensack
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Keyword5 values
clinical trial endpoints, electronic clinical outcome assessment, cardiac safety solutions, medical imaging core lab, precision motion wearables
Industry4 codes
1eCOA/ePRO/eDiary & Patient-Facing Data Collection
CodeHLACAOABPrimaryYes
2Clinical Trial Informatics (EDC/CTMS/eCOA/eTMF)
CodeHLAGAJAMPrimaryNo
3Clinical Trial Monitoring Support (On-site/Remote)
CodeHLAGACAGPrimaryNo
4Site & Investigator Platforms (Site Payments, Feasibility, Activation)
CodeHLACAOAJPrimaryNo
NAICS code2 codes
  • Other Scientific and Technical Consulting Services541690
  • Medical Equipment and Supplies Manufacturing3391
SIC code2 codes
  • Services-Prepackaged Software7372
  • Services-Misc Health & Allied Services, Nec8090
Product category
Clinical Trial Endpoint Technology
Social media profiles2 records
Marketing channels6 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, Marketing or Sales, Infrastructure
GTM typeB2B
B2B
Offering typeSoftware
Software
Core offering1 text field

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
Functional benefit
Problem solved
Quantifiable outcome1 of 4 values shown
  • 70% of FDA and EMA new drug approvals since 2015
+3 more records
Product and service8 records
1Cardiac Safety Solutions
CategoryCardiac Safety / ECG Monitoring
Description

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.

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

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.

3Medical Imaging Core Lab Services
CategoryMedical Imaging Core Lab
Description

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.

4Precision Motion / Opal System
CategoryWearable Sensor / Digital Endpoints
Description

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.

5Respiratory Solutions
CategoryRespiratory / Pulmonary Function Testing
Description

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.

6Trial Enablement Technology
CategoryClinical Trial Management Software
Description

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.

7Image Redact AI
CategoryAI / Imaging Privacy
Description

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.

8eC-SSRS (electronic Columbia Suicide Severity Rating Scale)
CategoryClinical Outcome Assessment / Safety
Description

Exclusive self-reported electronic Columbia Suicide Severity Rating Scale solution for monitoring suicidal ideation and behavior in clinical trials.

Scale indicator8 records

Each record includes

Type, Value, Description, Source

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

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.

TypeBroad incumbent
Description

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.

TypeDirect peer
Description

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.

TypeEmerging player
Description

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.

TypeBroad incumbent
Description

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.

TypeBroad incumbent
Description

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.

TypeBroad incumbent
Description

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.

TypeBroad incumbent
Description

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.

TypeEmerging player
Description

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.

TypeBroad incumbent
Description

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.

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 risks5 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

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
No

Docs URL, Description

AI maturity
App detail

Has app

Feature8 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles7 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 rounds2 records

Each record includes

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

Investors2 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&A

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 →

MedAvante

Clinical Trial Endpoint Technologymedavante.com

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.

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

  • Clinical trial endpoints
  • Electronic clinical outcome assessment
  • Cardiac safety solutions
  • Medical imaging core lab
  • Precision motion wearables

Where MedAvante is headquartered

Location

Headquarters

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 offering

Core 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 profile

Segments3 records

Ideal customer profiles3 records

MedAvante technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature8 records

MedAvante partnerships and signals

Strategic signal

Scale indicators8 records

Recent moves6 records

Expansion highlights6 records

MedAvante competitors and assessment

Company assessment

Direct 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 presence

MedAvante financial estimates

Financial estimate

Revenue estimate

Valuation estimate

MedAvante leadership team

Management profile

Number of profiles

Profiles7 records

MedAvante funding detail

Funding detail

Funding 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 investment

M&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.

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Live signals
PR NewswireWIRB-Copernicus Group (WCG) dokonuje nabycia firm MedAvante i ProPhaseWIRB-Copernicus Group (WCG) has completed the acquisition of MedAvante and ProPhase, two companies specializing in clinical trial solutions for behavioral health and central nervous system disorders. As part of the transaction, Dr. Jeffrey Litwin was appointed as the CEO of the combined entity to lead future operations. The deal aims to expand WCG's service portfolio by integrating MedAvante's electronic outcome assessment technologies with ProPhase's specialized measurement capabilities.PR NewswireWIRB-Copernicus Group (WCG) erwirbt MedAvante und ProPhaseWIRB-Copernicus Group (WCG) announced the acquisition of MedAvante and ProPhase to strengthen its position as a market leader in central nervous system and behavioral health clinical research. Dr. Jeffrey Litwin was appointed CEO of the combined entity, which aims to integrate technological solutions and scientific expertise to accelerate the development of life-saving therapies. Financial details of the transaction were not disclosed.PR NewswireWIRB-Copernicus Group (WCG) приобретает MedAvante и ProPhaseWIRB-Copernicus Group (WCG) announced the acquisition of MedAvante and ProPhase, two companies specializing in central nervous system (CNS) and mental health clinical assessment solutions, along with the appointment of Dr. Jeffrey Litwin as CEO of the combined organization. The transaction positions WCG as a market leader in CNS clinical trial services and technology products, offering clients a more comprehensive and integrated suite of solutions for launching clinical research. Financial terms of the deal were not disclosed.PR NewswireWIRB-Copernicus Group (WCG) acquiert MedAvante et ProPhaseWIRB-Copernicus Group (WCG) has acquired MedAvante and ProPhase, two companies specializing in central nervous system and behavioral health clinical trial assessments. The acquisition positions WCG as a leader in the expanding CNS clinical trial market by combining clinical services with technology solutions for improved signal detection. Dr. Jeffrey Litwin has been appointed CEO of the combined entity, which will continue operating under WCG's financial support and regulatory expertise.PR NewswireWIRB-Copernicus Group (WCG) se hace con MedAvante y ProPhaseWIRB-Copernicus Group (WCG) announced the acquisition of MedAvante and ProPhase, positioning itself as a leader in the behavioral and central nervous system health assessment market through clinical services and technology solutions that improve signal detection. Dr. Jeffrey Litwin has been appointed CEO of the combined organization, while WCG will provide corporate support to both acquired companies along with access to capital and complementary clinical and regulatory expertise. Financial terms of the transaction were not disclosed.PR NewswireSkupina WIRB-Copernicus Group (WCG) koupila společnosti MedAvante a ProPhaseWIRB-Copernicus Group (WCG), a leading provider of clinical research solutions, announced the acquisition of MedAvante and ProPhase, positioning itself as a leader in the central nervous system (CNS) disorders and behavioral health assessment market. Dr. Jeffrey Litwin has been appointed as CEO of the combined entity, which will offer more comprehensive and integrated clinical trial startup solutions to clients. Financial details of the transaction were not disclosed.PR NewswireU. of Chicago Booth School Presents Distinguished Alumni Award to Amy EllisMedAvante, Inc. announced that its president and co-founder Amy Ellis will receive the Distinguished Alumni Award from the University of Chicago Booth School of Business for her entrepreneurial achievements. The award recognizes Ellis's role in developing MedAvante's technological innovations, including the Virgil eSource Platform, which transforms clinical trial data collection. This recognition highlights the company's impact on global clinical data services across more than 40 countries.PR NewswireAraclon Biotech Selects MedAvante Virgil Platform for Phase 2 Alzheimer's TrialAraclon Biotech has selected MedAvante's Virgil Investigative Study Platform for its upcoming Phase 2 clinical trial of the Alzheimer's treatment ABvac40. MedAvante will provide electronic clinical outcome assessment services and clinical expertise to ensure data quality and operational efficiency for this multinational study.PR NewswireMedAvante Names Ropacki Head of Research and DevelopmentMedAvante announced the appointment of Michael T. Ropacki, PhD, as Vice President of Research and Development, effective immediately. Ropacki joins from Janssen Research & Development (Johnson & Johnson), where he led dementia research programs including the CHARIOT-PRO cohort study. The appointment strengthens MedAvante's scientific leadership as it expands into new therapeutic areas beyond its traditional focus on mood and anxiety disorders.PR NewswireIan Neilson Joins MedAvante As Global IT LeaderMedAvante, Inc., a clinical data services company, announced the appointment of Ian C. Neilson as Senior Vice President, Global Information Technology to lead its growing IT operations supporting clinical science and signal detection capabilities. Neilson brings over 19 years of senior IT executive experience, most recently serving as Vice President, Technology and Innovation at Covance's Clinical Development Services division, which is now part of LabCorp Holdings. The appointment is intended to support MedAvante's expanded focus on clinical trial management and data collection capabilities, including its Virgil eSource platform.