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CorEvitas

Full company profile

uuid0006ef7

Namestring
CorEvitas
Legal namestring
Thermo Fisher Scientific Inc.
Websiteurl
corevitas.com
Company typeenum
Private
Founded yearint
2000
Descriptiontext

CorEvitas operates as a branded real-world evidence (RWE) business unit within PPD, which is itself part of Thermo Fisher Scientific (NYSE: TMO). The company builds and operates proprietary longitudinal clinical registries that capture clinician- and patient-reported data from routine clinical practice across six therapeutic areas: dermatology, gastroenterology, neurology, obesity, pregnancy, and rheumatology. The portfolio is anchored by more than 20 years of continuous data collection, approximately 500 investigator sites globally, and a patient cohort of roughly 100,000, with newly launched registries in systemic lupus erythematosus (February 2025) and Alzheimer's disease (December 2025) extending the footprint. Acquired subsidiaries Vestrum Health (retina EHR analytics, 2021) and Pregistry (pregnancy safety studies, 2022), along with PPD CorEvitas Precision Medicine as a sub-brand, round out the product surface.

The underlying platform is a multi-disease registry network in which investigator sites contribute structured longitudinal data that can be aggregated, analyzed, and licensed to biopharmaceutical customers. CorEvitas generates revenue through subscription-based access to registry data, custom observational-study and RWE services (including pregnancy and lactation studies, health economics, and patient-centered research), and ongoing registry network participation fees. Pricing is enterprise and quote-based with annual billing cadence, and the go-to-market is direct enterprise sales conducted through PPD's global commercial organization, targeting pharmaceutical and biotech companies that need regulatory-grade evidence for drug development, post-authorization safety studies, and label-expansion submissions. The primary customer segment is pharma and biotech, with secondary segments in healthcare providers and government/public health agencies.

CorEvitas was originally established in 2000, was supported by an Audax Private Equity financing round in December 2019, and is now a wholly-owned subsidiary within Thermo Fisher Scientific following PPD's 2016 acquisition by Thermo Fisher. The company's geographic footprint is global, with active operations across North America, Europe (UK), and Asia-Pacific (China and Japan), and the recently launched international Alzheimer's registry indicates continued expansion beyond its historically US-anchored base.

Short descriptiontext

CorEvitas, a PPD/Thermo Fisher Scientific business unit, operates proprietary longitudinal clinical registries delivering regulatory-grade real-world evidence to pharmaceutical and biotech customers across six therapeutic areas, covering 500+ investigator sites and ~100,000 patients.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
251–500
akta.pro rankint
HeadquartersWaltham, United States
HQ citystring
Waltham
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
real-world evidence, clinical registries, longitudinal patient data, post-authorization studies, pharmacovigilance analytics
Industry2 codes
1Imaging & Cardiac Safety Core Labs (ECOG/EEG/ECG)
CodeHLAGAAAJPrimaryYes
2Specialty & Biomarker Laboratory Services (Immunoassays/Flow/Cytometry)
CodeHLAGAEABPrimaryNo
NAICS code1 code
  • Other Scientific and Technical Consulting Services54169
SIC code2 codes
  • Services-Health Services8000
  • Services-Misc Health & Allied Services, Nec8090
Product category
Real-World Evidence & Clinical Registry Data Services
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model3 records
1Clinical Registry Data Access
TypeSubscription Recurring
Description

Subscription-based access to proprietary longitudinal registry data for pharmaceutical and biotech companies conducting drug development, post-authorization safety studies, and real-world evidence generation.

ppd.com
2Observational Studies and RWE Services
TypeProfessional Services
Description

Custom study design and real-world evidence generation services including pregnancy and lactation studies, health economics, and patient-centered research.

ppd.com
3Registry Network Participation
TypeSubscription Recurring
Description

Engagement of investigator sites and physicians in registry networks, creating recurring data collection and study opportunities.

ppd.com
Marketing channels3 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
Pricing details1 tier
1Custom enterprise agreements based on data scope, therapeutic area, and study requirements
ModelSubscriptionBilling cadenceAnnual
Notes

Quote-based pricing tailored to customer requirements. No public pricing tiers available.

ppd.com
GTM typeB2B
B2B
Offering typeServices
Services
Brand1 record
1PPD CorEvitas Clinical Registries
Description

Proprietary real-world data registries covering dermatology, gastroenterology, neurology, obesity, pregnancy, and rheumatology therapeutic areas

ppd.com
Core offering1 text field

CorEvitas operates a portfolio of proprietary longitudinal clinical registries that collect regulator-grade clinician- and patient-reported real-world data across dermatology, gastroenterology, neurology, obesity, pregnancy, and rheumatology therapeutic areas. It sells subscription-based access to this registry data and delivers custom observational studies, post-authorization safety studies, pregnancy and lactation research, and patient-centered evidence services to pharmaceutical and biotech customers. Supporting offerings include precision medicine real-world data and retina EHR analytics via the acquired Vestrum Health platform.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 2 values shown
  • 500+ investigator sites and 100,000 patients across registry portfolio
+1 more record
Product overview1 text field

CorEvitas (operating as PPD CorEvitas under Thermo Fisher Scientific) is a multi-product platform offering proprietary longitudinal clinical registries. The core offering is the PPD CorEvitas Clinical Registries platform with over 20 years of proprietary data collection, which includes disease-specific registries across Dermatology, Gastroenterology, Neurology, Obesity, Pregnancy, and Rheumatology. The portfolio includes acquired brands such as Vestrum Health (retina EHR data analytics) and Pregistry (pregnancy safety studies). Additional offerings include PPD CorEvitas Precision Medicine for targeted therapeutic approaches. Together, these products enable regulatory-grade real-world evidence generation for pharmaceutical and biotech companies.

Product and service1 record
1PPD CorEvitas Clinical Registries
Scale indicator4 records

Each record includes

Type, Value, Description, Source

Partnership1 partner
Strategic tierCoreTypeOthers
Description

CorEvitas operates as a subsidiary/business unit within PPD, which is part of Thermo Fisher Scientific. The integration provides access to Thermo Fisher's full-service clinical research organization capabilities, laboratory services, and global infrastructure.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Largest global CRO and real-world evidence provider, offering proprietary datasets, observational studies and analytics services to biopharma. Overlaps directly with CorEvitas in registry-based RWE and longitudinal clinical data.

TypeOthers
Description

EHR vendor with real-world data offerings derived from its installed provider base. Not a direct CRO competitor but a data infrastructure peer whose EHR-extracted datasets compete for the same RWE buyer budgets.

TypeDirect peer
Description

Oncology-focused real-world evidence company (acquired by Roche) that aggregates EHR data from oncology practices. Comparable as a longitudinal disease-specific RWE platform serving biopharma for drug development and regulatory submissions.

TypeDirect peer
Description

Healthcare data and analytics platform providing real-world data infrastructure and analytics to providers, payers and life sciences. Comparable in selling longitudinal clinical data assets to biopharma.

TypeDirect peer
Description

Global CRO with established real-world evidence, post-marketing and observational research capabilities. Comparable business model and biopharma customer base to CorEvitas.

TypeDirect peer
Description

Major global CRO with real-world evidence and late-phase research capabilities post-PRA Health Sciences acquisition. Competes directly for biophara real-world data and post-authorization study contracts.

TypeDirect peer
Description

Biopharma solutions organization offering clinical development and real-world evidence services. Directly competes for biopharma RWE and observational study engagements.

TypeBroad incumbent
Description

Large IT services firm with healthcare data, real-world evidence and life sciences analytics offerings. Competes for biopharma RWE and clinical data engagements, particularly with payer and provider data sources.

TypeBroad incumbent
Description

Massive healthcare data and analytics business combining claims, EHR and pharmacy data. Broad incumbent offering real-world evidence at greater scale than CorEvitas, often competing for the same biopharma RWE budget.

TypeBroad incumbent
Description

Clinical trial technology and data platform serving biopharma with trial data capture, analytics and real-world data capabilities. Adjacent offering set to CorEvitas registries within the same sponsor buyer.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat5 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

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

Feature4 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles11 records

Each record includes

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

Subsidiaries2 records

Each record includes

Name, Acquired on, Relationship type, Type, Business focus

No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds1 record

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&A4 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 →

CorEvitas

Real-World Evidence & Clinical Registry Data Servicescorevitas.com

CorEvitas, a PPD/Thermo Fisher Scientific business unit, operates proprietary longitudinal clinical registries delivering regulatory-grade real-world evidence to pharmaceutical and biotech customers across six therapeutic areas, covering 500+ investigator sites and ~100,000 patients.

What CorEvitas does

CorEvitas operates as a branded real-world evidence (RWE) business unit within PPD, which is itself part of Thermo Fisher Scientific (NYSE: TMO). The company builds and operates proprietary longitudinal clinical registries that capture clinician- and patient-reported data from routine clinical practice across six therapeutic areas: dermatology, gastroenterology, neurology, obesity, pregnancy, and rheumatology. The portfolio is anchored by more than 20 years of continuous data collection, approximately 500 investigator sites globally, and a patient cohort of roughly 100,000, with newly launched registries in systemic lupus erythematosus (February 2025) and Alzheimer's disease (December 2025) extending the footprint. Acquired subsidiaries Vestrum Health (retina EHR analytics, 2021) and Pregistry (pregnancy safety studies, 2022), along with PPD CorEvitas Precision Medicine as a sub-brand, round out the product surface.

The underlying platform is a multi-disease registry network in which investigator sites contribute structured longitudinal data that can be aggregated, analyzed, and licensed to biopharmaceutical customers. CorEvitas generates revenue through subscription-based access to registry data, custom observational-study and RWE services (including pregnancy and lactation studies, health economics, and patient-centered research), and ongoing registry network participation fees. Pricing is enterprise and quote-based with annual billing cadence, and the go-to-market is direct enterprise sales conducted through PPD's global commercial organization, targeting pharmaceutical and biotech companies that need regulatory-grade evidence for drug development, post-authorization safety studies, and label-expansion submissions. The primary customer segment is pharma and biotech, with secondary segments in healthcare providers and government/public health agencies.

CorEvitas was originally established in 2000, was supported by an Audax Private Equity financing round in December 2019, and is now a wholly-owned subsidiary within Thermo Fisher Scientific following PPD's 2016 acquisition by Thermo Fisher. The company's geographic footprint is global, with active operations across North America, Europe (UK), and Asia-Pacific (China and Japan), and the recently launched international Alzheimer's registry indicates continued expansion beyond its historically US-anchored base.

CorEvitas firmographics

Firmographics
Name
CorEvitas
Legal name
Thermo Fisher Scientific Inc.
Website
https://corevitas.com
Company type
Private
Founded year
2000
Operating status
Operating
Headcount range
251–500 employees
Short description
CorEvitas, a PPD/Thermo Fisher Scientific business unit, operates proprietary longitudinal clinical registries delivering regulatory-grade real-world evidence to pharmaceutical and biotech customers across six therapeutic areas, covering 500+ investigator sites and ~100,000 patients.
Ownership category
akta.pro rank

CorEvitas industry classification

Industry
Product category
Real-World Evidence & Clinical Registry Data Services
NAICS
Other Scientific and Technical Consulting Services (54169)
SIC
Services-Health Services (8000), Services-Misc Health & Allied Services, Nec (8090)
akta.pro primary industry
Imaging & Cardiac Safety Core Labs (ECOG/EEG/ECG) (HLAGAAAJ)
akta.pro secondary industry
Specialty & Biomarker Laboratory Services (Immunoassays/Flow/Cytometry) (HLAGAEAB)

Keywords

  • Real-world evidence
  • Clinical registries
  • Longitudinal patient data
  • Post-authorization studies
  • Pharmacovigilance analytics

Where CorEvitas is headquartered

Location

Headquarters

HQ city
Waltham
HQ country
United States
HQ region
North America

Offices1 record

Markets served

CorEvitas 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. Clinical Registry Data Access: Subscription-based access to proprietary longitudinal registry data for pharmaceutical and biotech companies conducting drug development, post-authorization safety studies, and real-world evidence generation.
  2. Observational Studies and RWE Services: Custom study design and real-world evidence generation services including pregnancy and lactation studies, health economics, and patient-centered research.
  3. Registry Network Participation: Engagement of investigator sites and physicians in registry networks, creating recurring data collection and study opportunities.

Pricing tiers

ModelBillingPrice
SubscriptionAnnualCustom enterprise agreements based on data scope, therapeutic area, and study requirements

Go-to-market motion1 record

Distribution channels1 record

Marketing channels3 records

CorEvitas product offering

Product offering

Core offering

CorEvitas operates a portfolio of proprietary longitudinal clinical registries that collect regulator-grade clinician- and patient-reported real-world data across dermatology, gastroenterology, neurology, obesity, pregnancy, and rheumatology therapeutic areas. It sells subscription-based access to this registry data and delivers custom observational studies, post-authorization safety studies, pregnancy and lactation research, and patient-centered evidence services to pharmaceutical and biotech customers. Supporting offerings include precision medicine real-world data and retina EHR analytics via the acquired Vestrum Health platform.

Product overview

CorEvitas (operating as PPD CorEvitas under Thermo Fisher Scientific) is a multi-product platform offering proprietary longitudinal clinical registries. The core offering is the PPD CorEvitas Clinical Registries platform with over 20 years of proprietary data collection, which includes disease-specific registries across Dermatology, Gastroenterology, Neurology, Obesity, Pregnancy, and Rheumatology. The portfolio includes acquired brands such as Vestrum Health (retina EHR data analytics) and Pregistry (pregnancy safety studies). Additional offerings include PPD CorEvitas Precision Medicine for targeted therapeutic approaches. Together, these products enable regulatory-grade real-world evidence generation for pharmaceutical and biotech companies.

Differentiator

Problem solved

Functional benefit

Brands

  • PPD CorEvitas Clinical Registries: Proprietary real-world data registries covering dermatology, gastroenterology, neurology, obesity, pregnancy, and rheumatology therapeutic areas

Products and services

  • PPD CorEvitas Clinical Registries

Quantifiable outcome

  • 500+ investigator sites and 100,000 patients across registry portfolio
  • +1 more outcomes

Companies that use CorEvitas

Customer profile

Segments3 records

Ideal customer profiles3 records

CorEvitas technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature4 records

CorEvitas partnerships and signals

Strategic signal

Partnerships

One partnership is on record.

  • Thermo Fisher ScientificcoreOthersCorEvitas operates as a subsidiary/business unit within PPD, which is part of Thermo Fisher Scientific. The integration provides access to Thermo Fisher's full-service clinical research organization capabilities, laboratory services, and global infrastructure.

Scale indicators4 records

Recent moves6 records

Expansion highlights5 records

CorEvitas competitors and assessment

Company assessment

Direct peers

  • IQVIA: Largest global CRO and real-world evidence provider, offering proprietary datasets, observational studies and analytics services to biopharma. Overlaps directly with CorEvitas in registry-based RWE and longitudinal clinical data.
  • Flatiron Health: Oncology-focused real-world evidence company (acquired by Roche) that aggregates EHR data from oncology practices. Comparable as a longitudinal disease-specific RWE platform serving biopharma for drug development and regulatory submissions.
  • Health Catalyst: Healthcare data and analytics platform providing real-world data infrastructure and analytics to providers, payers and life sciences. Comparable in selling longitudinal clinical data assets to biopharma.
  • Parexel International: Global CRO with established real-world evidence, post-marketing and observational research capabilities. Comparable business model and biopharma customer base to CorEvitas.
  • ICON plc: Major global CRO with real-world evidence and late-phase research capabilities post-PRA Health Sciences acquisition. Competes directly for biophara real-world data and post-authorization study contracts.
  • Syneos Health: Biopharma solutions organization offering clinical development and real-world evidence services. Directly competes for biopharma RWE and observational study engagements.

Others

  • Veradigm (formerly Allscripts): EHR vendor with real-world data offerings derived from its installed provider base. Not a direct CRO competitor but a data infrastructure peer whose EHR-extracted datasets compete for the same RWE buyer budgets.

Broad incumbents

  • Cognizant (TriZetto / RWE Services): Large IT services firm with healthcare data, real-world evidence and life sciences analytics offerings. Competes for biopharma RWE and clinical data engagements, particularly with payer and provider data sources.
  • Optum (UnitedHealth Group): Massive healthcare data and analytics business combining claims, EHR and pharmacy data. Broad incumbent offering real-world evidence at greater scale than CorEvitas, often competing for the same biopharma RWE budget.
  • Medidata Solutions (Dassault Systèmes): Clinical trial technology and data platform serving biopharma with trial data capture, analytics and real-world data capabilities. Adjacent offering set to CorEvitas registries within the same sponsor buyer.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat5 records

Key risks6 records

Key highlights6 records

Customer concentration

CorEvitas social profiles

Digital presence

CorEvitas financial estimates

Financial estimate

Revenue estimate

Valuation estimate

CorEvitas leadership team

Management profile

Number of profiles

Profiles11 records

CorEvitas subsidiaries and ownership

Company hierarchy

Subsidiaries2 records

CorEvitas funding detail

Funding detail

Funding overview

Funding rounds1 record

Investors2 records

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

CorEvitas M&A and investment

M&A and investment

M&A4 records

Investments

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

Frequently asked questions about CorEvitas

What does CorEvitas do?

CorEvitas operates a portfolio of proprietary longitudinal clinical registries that collect regulator-grade clinician- and patient-reported real-world data across dermatology, gastroenterology, neurology, obesity, pregnancy, and rheumatology therapeutic areas. It sells subscription-based access to this registry data and delivers custom observational studies, post-authorization safety studies, pregnancy and lactation research, and patient-centered evidence services to pharmaceutical and biotech customers. Supporting offerings include precision medicine real-world data and retina EHR analytics via the acquired Vestrum Health platform.

Is CorEvitas a public or private company?

CorEvitas is a private company. It is classified as corporate owned and is currently operating.

When was CorEvitas founded?

CorEvitas was founded in 2000. It employs 251 to 500 people.

Where is CorEvitas based?

CorEvitas is headquartered in Waltham, United States, in the North America region.

How does CorEvitas make money?

Three revenue lines are on record. Clinical Registry Data Access are the primary driver. The others are observational Studies and RWE Services and registry Network Participation.

Who are CorEvitas's main competitors?

Direct peers on record are IQVIA, Flatiron Health, Health Catalyst, Parexel International, ICON plc and Syneos Health. Veradigm (formerly Allscripts) is listed as an others. Broad incumbents are Cognizant (TriZetto / RWE Services), Optum (UnitedHealth Group) and Medidata Solutions (Dassault Systèmes).

Does CorEvitas have an API?

No public API is recorded for CorEvitas.

What industry is CorEvitas in?

CorEvitas's product category is Real-World Evidence & Clinical Registry Data Services. Its primary akta.pro industry code is HLAGAAAJ, Imaging & Cardiac Safety Core Labs (ECOG/EEG/ECG), with a secondary code of HLAGAEAB, Specialty & Biomarker Laboratory Services (Immunoassays/Flow/Cytometry). Its NAICS code is 54169 and its SIC code is 8000.

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Live signals
FinancialContent Business PageArticles from Thermo FisherThermo Fisher Scientific announced on February 26, 2025 the launch of the CorEvitas Systemic Lupus Erythematosus Registry, a multi-center prospective registry designed to collect real-world clinical data about SLE through a rheumatology physician network. The registry aims to address critical gaps in understanding the safety and effectiveness of treatments for this chronic autoimmune disease that can damage skin, joints, blood, and internal organs including the kidneys, heart, brain, and lungs. By capturing clinician and patient insights, the initiative seeks to support evidence-based decisions for current and future SLE therapies.DrugdiscoverytrendsThermo Fisher launches obesity registry to track real-world treatment outcomesThermo Fisher Scientific has enrolled the first patient in the PPD CorEvitas Obesity Registry, a prospective observational study designed to generate real-world evidence on obesity treatments including GLP-1 receptor agonists. The registry will track treatment persistence, safety, tolerability concerns, and patient-reported outcomes across more than 500 investigator sites, addressing a significant data gap as industry analyses show 30% of patients on GLP-1 therapy stop within four weeks and only 8% remain at three years. The company describes the registry as regulatory-grade, with structured data capture designed to support post-authorization safety studies that regulators, payers, and prescribers increasingly require for obesity therapies.BioSpaceThermo Fisher Scientific Launches PPD CorEvitas Alzheimer’s Disease Registry to Advance Real-World Evidence in Neurodegenerative CareThermo Fisher Scientific announced the enrollment of the first patient in its new PPD CorEvitas Alzheimer's Disease Registry, an international initiative designed to generate robust real-world data on Alzheimer's therapy outcomes including safety monitoring, treatment patterns, and clinical effectiveness. The registry will collect longitudinal clinician-reported data from routine practice across multiple countries to support regulatory-grade evidence for drug evaluations and post-authorization safety studies. The initiative expands Thermo Fisher's portfolio of disease registries, which currently span over 500 investigator sites and 100,000 patients globally.BioSpaceThermo Fisher Scientific Launches CorEvitas Clinical Registry in Myasthenia Gravis, a Rare Autoimmune DisorderThermo Fisher Scientific announced the enrollment of the first patient in the new PPD CorEvitas Myasthenia Gravis Registry, a nationwide clinical data collection initiative in the United States. The registry aims to study disease progression and evaluate the safety and effectiveness of existing and emerging therapies for this rare autoimmune disorder. This launch marks the 14th independent registry from PPD CorEvitas Clinical Registries.StellarmrReal-World Evidence Market Size, Share & Growth Trends 2025-2032The global Real-World Evidence market was valued at USD 1.81 billion in 2024 and is projected to grow at a CAGR of 14.3% to reach USD 5.27 billion by 2032, driven by increasing adoption of AI-driven analytics and big data in healthcare for drug development and regulatory approvals. Key market developments include Thermo Fisher Scientific's acquisition of CorEvitas for USD 912.5 million in July 2023 and the FDA's issuance of guidelines for using real-world data in medical device and drug regulatory decisions. North America dominated the market in 2024 while Asia-Pacific is identified as the fastest-growing region, with major pharmaceutical companies increasingly leveraging real-world evidence solutions to reduce clinical trial costs and accelerate product approvals.Business Wire BlogAudax Private Equity Completes Sale of CorEvitasAudax Private Equity completed the sale of CorEvitas to Thermo Fisher, closing August 14, 2023. Audax invested in CorEvitas in December 2019 and saw it integrate five acquisitions and launch six clinical registries. The firm has since raised $5.25 billion for its successor fund.BenzingaThermo Fisher Acquires Audax-Backed CorEvitas For Over $900M - Thermo Fisher Scientific (NYSE:TMO)Thermo Fisher Scientific Inc agreed to acquire CorEvitas LLC from Audax Private Equity for $912.5 million in cash, with CorEvitas providing regulatory-grade real-world evidence solutions to pharmaceutical and biotechnology companies. CorEvitas manages 12 registries including nine autoimmune and inflammatory syndicated registries, spanning over 400 investigator sites and 100,000 patients followed longitudinally, with expected 2023 revenue of $110 million. The transaction, expected to close by end of 2023, will be immediately accretive to adjusted earnings per share by $0.03 in 2024 and will become part of Thermo Fisher's Laboratory Products and Biopharma Services segment.PR NewswireThe SPHERES Registry for NMOSD Patients Launches Precision Medicine ProgramCorEvitas, LLC and The Guthy-Jackson Charitable Foundation announced that the SPHERES Registry is now collecting biospecimens from consented participants to advance precision medicine research for Neuromyelitis Optica Spectrum Disorder (NMOSD). The biospecimen initiative targets over 300 participants and will pair with the registry's longitudinal clinical data to establish a unique research dataset for developing improved diagnostic testing and treatment options. The program aims to optimize treatment efficacy and safety for this rare autoimmune disease, which affects at least 15,000 people in the U.S. and hundreds of thousands worldwide.PR NewswireCorEvitas Launches its Ninth Clinical Registry and First of Its Kind in Alopecia AreataCorEvitas, LLC has launched and begun recruiting patients for a first-of-its-kind Alopecia Areata Safety and Effectiveness Registry, marking its ninth clinical registry focused on autoimmune and inflammatory diseases. The registry will collect longitudinal real-world data on disease severity, treatment outcomes, and the safety of JAK inhibitors and other novel therapies for Alopecia Areata, a condition affecting approximately 2 in 1,000 people in the U.S. and over 100 million worldwide. The company has partnered with clinical experts from Yale School of Medicine and Harvard Medical School to guide the research using regulatory-grade protocols.PR NewswireCorEvitas LLC Expands into Pregnancy with the Acquisition of Pregistry, LLCCorEvitas LLC has acquired Pregistry, LLC to expand its pharmacovigilance services into pregnancy safety studies and fulfill global regulatory requirements. This transaction marks CorEvitas' fifth acquisition, adding syndicated pregnancy observational studies to its real-world evidence portfolio. The deal was announced on November 21, 2022, with specific financial terms remaining undisclosed.