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New England IRB (acquired by WCG IRB)

Full company profile

uuid004ylif

Namestring
New England IRB (acquired by WCG IRB)
Legal namestring
WCG Clinical
Websiteurl
neirb.com
Company typeenum
Private
Founded yearstring
-
Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
1–10
akta.pro rankint
HeadquartersNot explicitly stated, United States
HQ citystring
Not explicitly stated
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices2 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
IRB review services, clinical trial ethics, biosafety committee review, clinical research compliance, independent ethical review
Industry2 codes
1Clinical Research Ethics & Human Subjects Protection Authorities (IRB/REC Oversight)
CodeHLAJACAGPrimaryYes
2Research Administration & Compliance (Sponsored Programs, IRB/REB)
CodeEDADAKAHPrimaryNo
NAICS code1 code
  • Other Scientific and Technical Consulting Services54169
SIC code1 code
  • Services-Misc Health & Allied Services, Nec8090
Product category
Institutional Review Board (IRB) Services
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model1 record
1IRB Review Services
TypeSubscription Recurring
Description

WCG generates revenue through professional IRB (Institutional Review Board) review services for clinical trials. Revenue is derived from reviewing protocols and research documents for pharmaceutical companies, biotech startups, medical device companies, CROs, and academic institutions. Services include standard IRB review, IRB+ premium expedited service, and specialized reviews for Phase I, pediatric, biologics, social/behavioral research. The company operates 12 hours a day, 7 days a week processing reviews.

wcgclinical.com
Marketing channels8 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
Pricing details2 tiers
1Standard IRB Review
ModelSubscriptionBilling cadenceAnnual
Notes

Standard IRB review services with defined turnaround times - less than 6 days for new protocol determinations, less than 2 days for new site determinations.

wcgclinical.com
2IRB+ Premium Service
ModelSubscriptionBilling cadenceMulti-year contract
Notes

Accelerated processing and white-glove service for studies requiring expedited review and enhanced support.

wcgclinical.com
GTM typeB2B
B2B
Offering typeServices
Services
Brand1 of 2 records shown
1IRB+
Description

Streamlined ethical review service for accelerated processing and white-glove service

wcgclinical.com
+1 more record
Core offering1 text field

WCG IRB provides independent ethical review services for clinical research protocols on behalf of pharmaceutical companies, biotech startups, medical device companies, CROs, and academic institutions. A board of nearly 200 IRB experts, augmented by an expert clinical advisory network, processes reviews 12 hours a day, 7 days per week, delivering new protocol determinations in less than 6 days and new site determinations in less than 2 days. The offering is supported by the ClinSphere® technology platform integrating eReview Manager, IRBNet, InvestigatorSpace®, AIMS®, Total Enrollment, Total Feasibility, eResearch Enterprise CTMS, CTLS, ClinSphere Trial IntelX™, and Latitude.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 3 values shown
  • Less than 6 days for new protocol determinations
+2 more records
Product overview1 text field

WCG IRB operates as a unified platform-plus-modules architecture centered on its core IRB Review service. The primary platform, ClinSphere®, integrates multiple technology solutions including eReview Manager, IRBNet, InvestigatorSpace®, AIMS®, Total Enrollment, Total Feasibility, eResearch Enterprise CTMS, Clinical Trial Listing Service (CTLS), ClinSphere Trial IntelX™, and Latitude. Premium service tiers include IRB+ for accelerated processing and specialized review services for pharmaceuticals, medical devices, biologics, Phase I trials, pediatrics, and social/behavioral research. Additional offerings include IBC Review, Endpoint Adjudication Committee, Data Monitoring Committees, WCG Site Network, Total Training, and Safety Letter Distribution.

Product and service26 records
1WCG IRB Review
CategoryIRB Review Services
Description

Independent central IRB ethical review service for clinical research protocols across all study phases and therapeutic areas, for sponsors, CROs, medical device companies, biotech startups, and academic institutions.

2IBC Review
CategoryBiosafety Committee Review
Description

Independent Institutional Biosafety Committee review for clinical studies involving biologics, cell therapy, gene therapy, stem cells, viral vectors, and gene transfer protocols.

3Endpoint Adjudication Committee
CategoryClinical Trial Committee Services
Description

Independent committee service that evaluates and adjudicates clinical trial endpoints for sponsors requiring unbiased endpoint assessment.

4Data Monitoring Committees
CategoryClinical Trial Committee Services
Description

Independent Data (Safety) Monitoring Committee service that oversees clinical trial data and ensures participant safety throughout the study.

5Total Training
CategoryClinical Research Training
Description

Clinical trial training solutions for research site staff and investigative personnel to support compliance and protocol adherence.

6Safety Letter Distribution
CategorySafety Communications
Description

Distribution service for safety communications from sponsors to clinical trial sites and investigators.

7WCG Site Network
CategorySite Network Services
Description

Network of clinical research sites used by sponsors and CROs to accelerate site onboarding and study activation.

8ClinSphere®
CategoryClinical Research Technology Platform
Description

Unified technology platform that integrates WCG's clinical research solutions, including IRB review, site network management, and analytics tools.

9eReview Manager
CategoryIRB Submission Platform
Description

Online platform for submitting studies to WCG IRB, tracking reviews, and managing IRB documentation in real time.

10IRBNet
CategoryIRB Document Management
Description

Technology platform for IRB document management and submission tracking.

11InvestigatorSpace® Training & Safety Portal
CategoryInvestigator Training and Safety
Description

Training and safety communication portal for clinical research investigators.

12AIMS®
CategoryClinical Research Analytics
Description

Analytics and information management system for clinical research data.

13Total Enrollment
CategoryParticipant Recruitment Technology
Description

Participant recruitment and enrollment technology solution for clinical trials.

14Total Feasibility
CategoryStudy Feasibility Technology
Description

Study feasibility assessment technology for evaluating site capabilities and study requirements.

15eResearch Enterprise CTMS
CategoryClinical Trial Management System
Description

Clinical trial management system for study operations and oversight.

16Clinical Trial Listing Service (CTLS)
CategoryClinical Trial Listing Services
Description

Service for listing and managing clinical trial information.

17ClinSphere Trial IntelX™
CategoryTrial Intelligence and Analytics
Description

Trial intelligence and analytics solution for clinical research benchmarking and performance management.

18Latitude
CategorySite Management and Collaboration Platform
Description

Platform for clinical research site management and collaboration.

19Recruitment & Retention
CategoryParticipant Recruitment and Retention
Description

Solutions to help sponsors overcome barriers and reach study enrollment goals faster through targeted recruitment and retention services.

20Benchmarking & Performance Management
CategoryData and Insights Services
Description

Benchmarking and performance management solutions for clinical research organizations.

21Quality & Compliance
CategoryQuality and Compliance Services
Description

Quality and compliance advisory and program support for clinical research organizations.

22Statistical Consulting
CategoryStatistical Consulting
Description

Statistical consulting solutions for clinical research data analysis and trial design.

23Diversity, Equity, & Inclusion
CategoryDEI in Clinical Research
Description

Solutions supporting diversity, equity, and inclusion across clinical research programs.

24Trial Design & Protocol Planning
CategoryTrial Design and Protocol Planning
Description

Trial design and protocol planning consulting service to help sponsors structure clinical research programs.

25Study Planning & Review
CategoryStudy Planning and Protocol Design
Description

Service to design protocols to protect participants and minimize risk prior to IRB submission.

26Therapeutic Area Solutions
CategoryTherapeutic Area Specialty Services
Description

Specialized IRB review and clinical research support across therapeutic areas including Hematology/Oncology, CNS, Cardiovascular, Metabolic, Infectious Disease, Dermatology, Immunology, and Gastroenterology.

Scale indicator7 records

Each record includes

Type, Value, Description, Source

Partnership1 partner
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2022-09-01
Description

WCG IRB expanded Phase I review services through partnership with Dr. Vince Clinical Research, enhancing capabilities for first-in-human studies. This partnership brings additional expertise in Phase I clinical trial review, with board members who are former Phase I investigators whose experience is invaluable for residential studies and complex pharmacology trials.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeBroad incumbent
Description

Parexel (including PPD) is a global CRO serving pharma and biotech sponsors across clinical operations, regulatory, and site services. It is also a named WCG customer, illustrating how CRO incumbents both partner and compete in adjacent IRB-adjacent workflows.

TypeBroad incumbent
Description

IQVIA is a global CRO and clinical research services incumbent offering protocol operations, site management, and regulatory/ethics coordination at scale. While not a pure IRB, it competes for sponsor budgets and increasingly bundles IRB-adjacent capabilities.

TypeDirect peer
Description

Advarra is a leading central IRB formed from the merger of Schulman IRB and Quorum Review, offering IRB, IBC, and HRPP services to sponsors, CROs, and academic institutions. It is the most direct head-to-head competitor to WCG IRB across enterprise review and oncology/genetics protocols.

TypeBroad incumbent
Description

Fortrea, spun out from Labcorp, is a global clinical development and commercialization services incumbent. It competes for sponsor R&D budgets and provides overlapping clinical operations and central lab capabilities relevant to WCG's broader platform.

TypeBroad incumbent
Description

Syneos Health is a fully integrated biopharmaceutical solutions organization offering clinical and commercial services across development, site, and recruitment. It is comparable to the broader WCG platform footprint beyond pure IRB review.

TypeDirect peer
Description

Sterling IRB is an AAHRPP-accredited central IRB serving academic, pharmaceutical, and CRO sponsors with protocol review and study management services. It competes directly with WCG on turnaround time, expertise, and accreditation.

TypeDirect peer
Description

Biomedical Research Alliance of New York (BRANY) provides IRB and HRPP services with strong academic medical center roots, including the Icahn School of Medicine at Mount Sinai. It is a directly comparable central IRB serving sponsors and academic institutions.

TypeBroad incumbent
Description

ICON is a global CRO offering clinical research, site activation, and central laboratory services to pharma and biotech sponsors. It overlaps with WCG's ClinSphere-enabling services (site, recruitment, feasibility) as part of a broader portfolio.

TypeDirect peer
Description

Copernicus Group IRB (CGI) is an AAHRPP-accredited central IRB providing independent ethical review for clinical research across pharmaceutical, biotech, and medical device sponsors. It is a direct alternative for sponsor review work.

TypeBroad incumbent
Description

Charles River is an established preclinical and clinical services incumbent serving pharma and biotech sponsors across discovery, safety, and clinical trial support. It overlaps with WCG in clinical operations and broader sponsor services.

Market position
Strengths4 records

Each record includes

Headline, Details, Source

Weaknesses4 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 highlights6 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers3 records

Each record includes

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

Segment7 records

Each record includes

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

Ideal customer profile5 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

Feature7 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
No data
Compliance10 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&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 →

New England IRB (acquired by WCG IRB)

Institutional Review Board (IRB) Servicesneirb.com

New England IRB (acquired by WCG IRB) firmographics

Firmographics
Name
New England IRB (acquired by WCG IRB)
Legal name
WCG Clinical
Website
https://neirb.com
Company type
Private
Operating status
Operating
Headcount range
1–10 employees
Ownership category
akta.pro rank

New England IRB (acquired by WCG IRB) industry classification

Industry
Product category
Institutional Review Board (IRB) Services
NAICS
Other Scientific and Technical Consulting Services (54169)
SIC
Services-Misc Health & Allied Services, Nec (8090)
akta.pro primary industry
Clinical Research Ethics & Human Subjects Protection Authorities (IRB/REC Oversight) (HLAJACAG)
akta.pro secondary industry
Research Administration & Compliance (Sponsored Programs, IRB/REB) (EDADAKAH)

Keywords

  • IRB review services
  • Clinical trial ethics
  • Biosafety committee review
  • Clinical research compliance
  • Independent ethical review

Where New England IRB (acquired by WCG IRB) is headquartered

Location

Headquarters

HQ city
Not explicitly stated
HQ country
United States
HQ region
North America

Offices2 records

Markets served

New England IRB (acquired by WCG IRB) business model

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

Revenue model

  1. IRB Review Services: WCG generates revenue through professional IRB (Institutional Review Board) review services for clinical trials. Revenue is derived from reviewing protocols and research documents for pharmaceutical companies, biotech startups, medical device companies, CROs, and academic institutions. Services include standard IRB review, IRB+ premium expedited service, and specialized reviews for Phase I, pediatric, biologics, social/behavioral research. The company operates 12 hours a day, 7 days a week processing reviews.

Pricing tiers

ModelBillingPrice
SubscriptionAnnualStandard IRB Review
SubscriptionMulti-year contractIRB+ Premium Service

Go-to-market motion1 record

Distribution channels4 records

Marketing channels8 records

New England IRB (acquired by WCG IRB) product offering

Product offering

Core offering

WCG IRB provides independent ethical review services for clinical research protocols on behalf of pharmaceutical companies, biotech startups, medical device companies, CROs, and academic institutions. A board of nearly 200 IRB experts, augmented by an expert clinical advisory network, processes reviews 12 hours a day, 7 days per week, delivering new protocol determinations in less than 6 days and new site determinations in less than 2 days. The offering is supported by the ClinSphere® technology platform integrating eReview Manager, IRBNet, InvestigatorSpace®, AIMS®, Total Enrollment, Total Feasibility, eResearch Enterprise CTMS, CTLS, ClinSphere Trial IntelX™, and Latitude.

Product overview

WCG IRB operates as a unified platform-plus-modules architecture centered on its core IRB Review service. The primary platform, ClinSphere®, integrates multiple technology solutions including eReview Manager, IRBNet, InvestigatorSpace®, AIMS®, Total Enrollment, Total Feasibility, eResearch Enterprise CTMS, Clinical Trial Listing Service (CTLS), ClinSphere Trial IntelX™, and Latitude. Premium service tiers include IRB+ for accelerated processing and specialized review services for pharmaceuticals, medical devices, biologics, Phase I trials, pediatrics, and social/behavioral research. Additional offerings include IBC Review, Endpoint Adjudication Committee, Data Monitoring Committees, WCG Site Network, Total Training, and Safety Letter Distribution.

Differentiator

Problem solved

Functional benefit

Brands

  • IRB+: Streamlined ethical review service for accelerated processing and white-glove service
  • ClinSphere eReview Manager

Products and services

  • WCG IRB Review Independent central IRB ethical review service for clinical research protocols across all study phases and therapeutic areas, for sponsors, CROs, medical device companies, biotech startups, and academic institutions.
  • IBC Review Independent Institutional Biosafety Committee review for clinical studies involving biologics, cell therapy, gene therapy, stem cells, viral vectors, and gene transfer protocols.
  • Endpoint Adjudication Committee Independent committee service that evaluates and adjudicates clinical trial endpoints for sponsors requiring unbiased endpoint assessment.
  • Data Monitoring Committees Independent Data (Safety) Monitoring Committee service that oversees clinical trial data and ensures participant safety throughout the study.
  • Total Training Clinical trial training solutions for research site staff and investigative personnel to support compliance and protocol adherence.
  • Safety Letter Distribution Distribution service for safety communications from sponsors to clinical trial sites and investigators.
  • WCG Site Network Network of clinical research sites used by sponsors and CROs to accelerate site onboarding and study activation.
  • ClinSphere® Unified technology platform that integrates WCG's clinical research solutions, including IRB review, site network management, and analytics tools.
  • eReview Manager Online platform for submitting studies to WCG IRB, tracking reviews, and managing IRB documentation in real time.
  • IRBNet Technology platform for IRB document management and submission tracking.
  • InvestigatorSpace® Training & Safety Portal Training and safety communication portal for clinical research investigators.
  • AIMS® Analytics and information management system for clinical research data.
  • Total Enrollment Participant recruitment and enrollment technology solution for clinical trials.
  • Total Feasibility Study feasibility assessment technology for evaluating site capabilities and study requirements.
  • eResearch Enterprise CTMS Clinical trial management system for study operations and oversight.
  • Clinical Trial Listing Service (CTLS) Service for listing and managing clinical trial information.
  • ClinSphere Trial IntelX™ Trial intelligence and analytics solution for clinical research benchmarking and performance management.
  • Latitude Platform for clinical research site management and collaboration.
  • Recruitment & Retention Solutions to help sponsors overcome barriers and reach study enrollment goals faster through targeted recruitment and retention services.
  • Benchmarking & Performance Management Benchmarking and performance management solutions for clinical research organizations.
  • Quality & Compliance Quality and compliance advisory and program support for clinical research organizations.
  • Statistical Consulting Statistical consulting solutions for clinical research data analysis and trial design.
  • Diversity, Equity, & Inclusion Solutions supporting diversity, equity, and inclusion across clinical research programs.
  • Trial Design & Protocol Planning Trial design and protocol planning consulting service to help sponsors structure clinical research programs.
  • Study Planning & Review Service to design protocols to protect participants and minimize risk prior to IRB submission.
  • Therapeutic Area Solutions Specialized IRB review and clinical research support across therapeutic areas including Hematology/Oncology, CNS, Cardiovascular, Metabolic, Infectious Disease, Dermatology, Immunology, and Gastroenterology.

Quantifiable outcome

  • Less than 6 days for new protocol determinations
  • +2 more outcomes

Companies that use New England IRB (acquired by WCG IRB)

Customer profile

Named customers3 records

Segments7 records

Ideal customer profiles5 records

New England IRB (acquired by WCG IRB) technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature7 records

New England IRB (acquired by WCG IRB) partnerships and signals

Strategic signal

Partnerships

One partnership is on record.

  • Dr. Vince Clinical ResearchcoreStrategic or Co-development Partner · 1 September 2022WCG IRB expanded Phase I review services through partnership with Dr. Vince Clinical Research, enhancing capabilities for first-in-human studies. This partnership brings additional expertise in Phase I clinical trial review, with board members who are former Phase I investigators whose experience is invaluable for residential studies and complex pharmacology trials.

Scale indicators7 records

Recent moves6 records

Expansion highlights5 records

New England IRB (acquired by WCG IRB) competitors and assessment

Company assessment

Broad incumbents

  • Parexel: Parexel (including PPD) is a global CRO serving pharma and biotech sponsors across clinical operations, regulatory, and site services. It is also a named WCG customer, illustrating how CRO incumbents both partner and compete in adjacent IRB-adjacent workflows.
  • IQVIA: IQVIA is a global CRO and clinical research services incumbent offering protocol operations, site management, and regulatory/ethics coordination at scale. While not a pure IRB, it competes for sponsor budgets and increasingly bundles IRB-adjacent capabilities.
  • Labcorp Drug Development (Fortrea): Fortrea, spun out from Labcorp, is a global clinical development and commercialization services incumbent. It competes for sponsor R&D budgets and provides overlapping clinical operations and central lab capabilities relevant to WCG's broader platform.
  • Syneos Health: Syneos Health is a fully integrated biopharmaceutical solutions organization offering clinical and commercial services across development, site, and recruitment. It is comparable to the broader WCG platform footprint beyond pure IRB review.
  • ICON plc: ICON is a global CRO offering clinical research, site activation, and central laboratory services to pharma and biotech sponsors. It overlaps with WCG's ClinSphere-enabling services (site, recruitment, feasibility) as part of a broader portfolio.
  • Charles River Laboratories: Charles River is an established preclinical and clinical services incumbent serving pharma and biotech sponsors across discovery, safety, and clinical trial support. It overlaps with WCG in clinical operations and broader sponsor services.

Direct peers

  • Advarra: Advarra is a leading central IRB formed from the merger of Schulman IRB and Quorum Review, offering IRB, IBC, and HRPP services to sponsors, CROs, and academic institutions. It is the most direct head-to-head competitor to WCG IRB across enterprise review and oncology/genetics protocols.
  • Sterling IRB: Sterling IRB is an AAHRPP-accredited central IRB serving academic, pharmaceutical, and CRO sponsors with protocol review and study management services. It competes directly with WCG on turnaround time, expertise, and accreditation.
  • BRANY: Biomedical Research Alliance of New York (BRANY) provides IRB and HRPP services with strong academic medical center roots, including the Icahn School of Medicine at Mount Sinai. It is a directly comparable central IRB serving sponsors and academic institutions.
  • Copernicus Group IRB: Copernicus Group IRB (CGI) is an AAHRPP-accredited central IRB providing independent ethical review for clinical research across pharmaceutical, biotech, and medical device sponsors. It is a direct alternative for sponsor review work.

Market position

Strengths4 records

Weaknesses4 records

Competitive moat6 records

Key risks6 records

Key highlights6 records

Customer concentration

New England IRB (acquired by WCG IRB) social profiles

Digital presence

New England IRB (acquired by WCG IRB) compliance and trust

Trust signal

Compliance10 records

New England IRB (acquired by WCG IRB) financial estimates

Financial estimate

Revenue estimate

Valuation estimate

New England IRB (acquired by WCG IRB) leadership team

Management profile

Number of profiles

New England IRB (acquired by WCG IRB) funding detail

Funding detail

Funding overview

Funding rounds

Investors

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

New England IRB (acquired by WCG IRB) 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 New England IRB (acquired by WCG IRB)

What does New England IRB (acquired by WCG IRB) do?

WCG IRB provides independent ethical review services for clinical research protocols on behalf of pharmaceutical companies, biotech startups, medical device companies, CROs, and academic institutions. A board of nearly 200 IRB experts, augmented by an expert clinical advisory network, processes reviews 12 hours a day, 7 days per week, delivering new protocol determinations in less than 6 days and new site determinations in less than 2 days. The offering is supported by the ClinSphere® technology platform integrating eReview Manager, IRBNet, InvestigatorSpace®, AIMS®, Total Enrollment, Total Feasibility, eResearch Enterprise CTMS, CTLS, ClinSphere Trial IntelX™, and Latitude.

Is New England IRB (acquired by WCG IRB) a public or private company?

New England IRB (acquired by WCG IRB) is a private company. It is classified as unknown and is currently operating.

When was New England IRB (acquired by WCG IRB) founded?

New England IRB (acquired by WCG IRB) was founded in -1. It employs 1 to 10 people.

Where is New England IRB (acquired by WCG IRB) based?

New England IRB (acquired by WCG IRB) is headquartered in Not explicitly stated, United States, in the North America region.

How does New England IRB (acquired by WCG IRB) make money?

One revenue line is on record: IRB Review Services.

Who are New England IRB (acquired by WCG IRB)'s main competitors?

Broad incumbents on record are Parexel, IQVIA, Labcorp Drug Development (Fortrea), Syneos Health, ICON plc and Charles River Laboratories. Direct peers are Advarra, Sterling IRB, BRANY and Copernicus Group IRB.

Does New England IRB (acquired by WCG IRB) have an API?

No public API is recorded for New England IRB (acquired by WCG IRB).

What industry is New England IRB (acquired by WCG IRB) in?

New England IRB (acquired by WCG IRB)'s product category is Institutional Review Board (IRB) Services. Its primary akta.pro industry code is HLAJACAG, Clinical Research Ethics & Human Subjects Protection Authorities (IRB/REC Oversight), with a secondary code of EDADAKAH, Research Administration & Compliance (Sponsored Programs, IRB/REB). Its NAICS code is 54169 and its SIC code is 8090.

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