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CMX Research

Full company profile

uuid000s2sz

Namestring
CMX Research
Legal namestring
CMX Research Inc.
Websiteurl
cmxres.com
Company typeenum
Private
Founded yearint
1992
Descriptiontext

CMX Research Inc. is a privately held, niche Contract Research Organization headquartered in Oakville, Ontario, Canada. Founded in 1992 as a Site Management Organization, the company has evolved into a full-service CRO providing Phase I–IV clinical trial services for drug and medical device studies, with a stated specialty in urology and oncology. The business is founder-led by Dr. Richard Casey, MD, FRCS(C), an actively practicing urologist and principal investigator, whose clinical background positions CMX around protocol design quality and patient-friendly study execution rather than scale-driven volume.

The company's service portfolio is organized around four core offerings — Full Service CRO (project management, site monitoring, regulatory affairs, vendor procurement, medical writing, safety/medical monitoring, statistical analysis, protocol writing, and eDC data management), Investigator Network (clinical trial sites across Canada and the USA across community, hospital-based, and academic settings), Investigator-Led Trials support, and Monitoring Services (CRA-led SQV/SIV/IMV/COV visits) — supplemented by secondary services such as regulatory submissions to Health Canada and FDA, device trials, recruitment/advertising, and a newly added Pharmacovigilance module launched in 2024. Technology stack is conventional CRO tooling centred on electronic Data Capture (eDC) data management via third-party vendors; no proprietary AI/ML or platform-as-a-service components are disclosed.

CMX generates revenue on a professional-services, project-by-project basis through direct sales engagement with pharmaceutical organizations, biotech firms, and medical device manufacturers. Pricing is custom-tailored per study and not publicly disclosed. Target customers span large global pharma (Pfizer, Novartis, Roche, AstraZeneca, Bayer, Janssen, Lilly, Sanofi, BMS Canada, Amgen, AbbVie, among others), emerging biotech, device companies, and sub-contracted engagements with Tier-1 CROs (IQVIA, PPD, Icon, PRA Health Sciences, Syneos Health, Chiltern). Trials are executed across 13 countries, including Canada, the United States, and multiple European and Asian jurisdictions.

Short descriptiontext

CMX Research Inc. is a privately held, Oakville-based niche Contract Research Organization founded in 1992 that provides full-service Phase I-IV clinical trial management, monitoring, regulatory affairs, and data services for global pharmaceutical, biotech, and medical device sponsors, with a specialty in urology and oncology.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersOakville, Canada
HQ citystring
Oakville
HQ countrystring
Canada
HQ regionstring
North America
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
clinical research services, contract research organization, clinical trial management, pharmacovigilance services, site management organization
Industry6 codes
1Clinical CROs (Phase I–IV)
CodeHLAGAAAAPrimaryYes
2Clinical Trial Monitoring Support (On-site/Remote)
CodeHLAGACAGPrimaryNo
3Clinical Site Start-Up & Activation (Regulatory/Ethics/Contracts)
CodeHLAGACACPrimaryNo
4Regulatory Strategy & Global Submissions (IND/CTA/NDA/BLA/MAA)
CodeHLAGAKAAPrimaryNo
5Specialty Therapeutic-Area CROs (e.g., oncology/rare disease)
CodeHLAGAAALPrimaryNo
6Clinical Trial Informatics (EDC/CTMS/eCOA/eTMF)
CodeHLAGAJAMPrimaryNo
NAICS code2 codes
  • Research and Development in the Physical, Engineering, and Life Sciences54171
  • Scientific Research and Development Services5417
SIC code1 code
  • Services-Commercial Physical & Biological Research8731
Product category
Contract Research Organization (CRO) / Clinical Research Services
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model1 record
1Clinical Research Services
TypeProfessional Services
Description

CMX Research generates revenue through providing full-service CRO services including clinical trial management, monitoring, regulatory affairs, data management, and pharmacovigilance services for Phase I-IV clinical trials. Revenue is earned through service contracts with pharmaceutical companies, biotech firms, and device manufacturers.

cmxres.com
Marketing channels1 record

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, Operations, Technology or R&D, Marketing or Sales, Infrastructure
GTM typeB2B
B2B
Offering typeServices
Services
Core offering1 text field

CMX Research is a niche Contract Research Organization (CRO) that designs and executes Phase I-IV clinical trials for pharmaceutical, biotech, and medical device sponsors across urology, oncology, immunology, cardiology, dermatology, endocrinology, and respirology. The company delivers full-service clinical trial management including project management, site monitoring and training, regulatory affairs, vendor procurement, medical writing, safety and medical monitoring, statistical analysis, protocol writing, and eDC-based data management. Its services are anchored by the largest urology-oncology principal investigator network in Canada and the USA, and supplemented by recently launched Pharmacovigilance Services.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 4 values shown
  • Completed over 400 studies successfully since 1992
+3 more records
Product overview1 text field

CMX Research is a niche Contract Research Organization (CRO) that evolved from a Site Management Organization (SMO) founded in 1992. Its service portfolio is organized around four interconnected core offerings: Full Service CRO (spanning project management, site monitoring and training, regulatory affairs, vendor procurement, medical writing, safety/medical monitoring, statistical analysis, protocol writing and study design, and eDC data management), Investigator Network (providing access to clinical trial sites across Canada and the USA), Investigator-Led Trials (ILTs) support (covering study design through final report writing), and Monitoring Services (CRA-led visits from SQVs through COVs for Phase I–IV and BA/BE studies). These core services are supplemented by secondary offerings including protocol design, early-phase proof-of-concept studies, regulatory submissions to Health Canada and FDA, device trials, central advertising and recruitment, physician focus groups, and audits. A newly added Pharmacovigilance Services module rounds out the portfolio.

Product and service6 records
1Full Service CRO
CategoryFull Service CRO
Description

Comprehensive contract research organization services covering Phase I-IV clinical trials for pharmaceutical, biotech, and device sponsors, including project management, site monitoring, regulatory affairs, vendor procurement, medical writing, safety monitoring, statistical analysis, protocol writing, and eDC-based data management.

2Investigator Network
CategoryInvestigator Network
Description

Extensive network of clinical trial sites across Canada and the USA spanning community sites, hospital-based research organizations, and academic institutions, with a focus on urology and oncology principal investigators — described as the largest urology-oncology PI network in North America.

3Investigator-Led Trials (ILTs)
CategoryInvestigator-Led Trials Support
Description

Support services for investigator-initiated trials including study design and launch, study management, site selection and recruitment, budget-friendly pricing and grant support, strategic study support, data management and analysis, and final report writing.

4Monitoring Services
CategoryMonitoring Services
Description

Clinical trial monitoring conducted by trained and certified Clinical Research Associates (CRAs), including Site Qualification Visits (SQVs), Site Initiation Visits (SIVs), Interim Monitoring Visits (IMVs), and Close-Out Visits (COVs) for Phase I-IV and BA/BE studies.

5Secondary Services
CategorySupplementary CRO Services
Description

Additional services including protocol design and development, early phase / proof of concept studies, regulatory submissions to Health Canada and FDA, device trials, central advertising and recruitment services, call centre support, physician focus groups, and audits.

6Pharmacovigilance Services
CategoryPharmacovigilance
Description

Newly launched pharmacovigilance services for safety and adverse event monitoring in clinical trials, extending CMX's service portfolio into post-trial and ongoing safety surveillance.

Scale indicator5 records

Each record includes

Type, Value, Description, Source

Partnership21 partners
Strategic tierMinorTypeOthers
Description

Pharmaceutical company listed as a client partner of CMX Research for clinical trial services.

Strategic tierMinorTypeOthers
Description

Global pharmaceutical company listed as a client partner of CMX Research for clinical trial services.

Strategic tierMinorTypeOthers
Description

Global pharmaceutical company listed as a client partner of CMX Research for clinical trial services.

Strategic tierMinorTypeOthers
Description

Global pharmaceutical company listed as a client partner of CMX Research for clinical trial services.

Strategic tierMinorTypeOthers
Description

Global pharmaceutical company listed as a client partner of CMX Research for clinical trial services.

Strategic tierMinorTypeOthers
Description

Pharmaceutical company listed as a client partner of CMX Research for clinical trial services.

Strategic tierMinorTypeOthers
Description

Pharmaceutical company (Johnson & Johnson subsidiary) listed as a client partner of CMX Research for clinical trial services.

Strategic tierMinorTypeOthers
Description

Global pharmaceutical company listed as a client partner of CMX Research for clinical trial services.

Strategic tierMinorTypeOthers
Description

Global pharmaceutical company listed as a client partner of CMX Research for clinical trial services.

Strategic tierMinorTypeOthers
Description

Global pharmaceutical company listed as a client partner of CMX Research for clinical trial services.

Strategic tierMinorTypeOthers
Description

Global pharmaceutical company listed as a client partner of CMX Research for clinical trial services.

Strategic tierMinorTypeOthers
Description

Global pharmaceutical company listed as a client partner of CMX Research for clinical trial services.

Strategic tierMinorTypeOthers
Description

Global pharmaceutical company listed as a client partner of CMX Research for clinical trial services.

Strategic tierMinorTypeOthers
Description

Global pharmaceutical company listed as a client partner of CMX Research for clinical trial services.

Strategic tierMinorTypeOthers
Description

Pharmaceutical company listed as a client partner of CMX Research for clinical trial services.

Strategic tierMinorTypeChannel Partner/ Reseller/ Distributor
Description

CMX has worked with Chiltern as a CRO partner, providing clinical trial services.

Strategic tierMinorTypeChannel Partner/ Reseller/ Distributor
Description

CMX has collaborated with IQVIA as a CRO partner, providing clinical trial services.

18Icon
Strategic tierMinorTypeChannel Partner/ Reseller/ Distributor
Description

CMX has worked with Icon as a CRO partner, providing clinical trial services.

cmxres.com
19PPD
Strategic tierMinorTypeChannel Partner/ Reseller/ Distributor
Description

CMX has collaborated with PPD as a CRO partner, providing clinical trial services.

Strategic tierMinorTypeChannel Partner/ Reseller/ Distributor
Description

CMX has worked with PRA Health Sciences as a CRO partner, providing clinical trial services.

Strategic tierMinorTypeChannel Partner/ Reseller/ Distributor
Description

CMX has collaborated with Syneos Health as a CRO partner, providing clinical trial services.

Recent move5 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeEmerging player
Description

Mid-size specialty CRO focused on oncology and complex therapeutics — comparable to CMX on therapeutic specialization and small/mid CRO scale, though with broader geographic footprint.

TypeBroad incumbent
Description

Largest global CRO and a documented CMX channel-partner/sub-contractor. Overlaps with CMX's full-service Phase I-IV offerings but operates at vastly greater scale across all therapeutic areas.

TypeBroad incumbent
Description

Large clinical and commercial services CRO (post-spin Fortrea) and a documented CMX channel partner — competes across Phase I-IV with broader scale and integrated commercialization.

TypeBroad incumbent
Description

Top-3 global CRO (formed via PRA Health Sciences combination) and a documented CMX channel partner — competing broad CRO with full Phase I-IV capabilities that often sub-contracts site and monitoring work to specialists like CMX.

TypeDirect peer
Description

Specialty-focused CRO with therapeutic expertise in oncology, urology, rare disease and pediatrics — directly comparable on therapeutic specialization, mid-scale full-service delivery, and PI-relationship-driven model.

TypeDirect peer
Description

Mid-size, therapeutically-focused full-service CRO with a reputation for medical/scientific depth and investigator-driven execution — directly comparable to CMX's clinical-led, specialty-therapy model, but at substantially greater scale.

TypeDirect peer
Description

Mid-size specialty CRO with strong therapeutic-area depth in oncology, urology and CNS — competes head-to-head with CMX for specialty Phase II/III work and shares the same medical-led positioning.

TypeDirect peer
Description

Mid-size full-service CRO with oncology and specialty therapeutic expertise and a mix of sponsor and biotech clients — closely comparable on service breadth and therapeutic emphasis.

TypeEmerging player
Description

Niche CRO with early-phase clinical pharmacology and BA/BE expertise — directly comparable to CMX's BA/BE monitoring line and Phase I capability, with similar size and specialty positioning.

TypeBroad incumbent
Description

Top-5 global CRO within Thermo Fisher and a documented CMX channel partner — broad full-service CRO competing with CMX in oncology/urology sponsor work, often leveraging specialists for site execution.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat4 records

Each record includes

Type, Details

Key risks7 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers33 records

Each record includes

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

Segment4 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
No
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles1 record

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 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 →

CMX Research

Contract Research Organization (CRO) / Clinical Research Servicescmxres.com

CMX Research Inc. is a privately held, Oakville-based niche Contract Research Organization founded in 1992 that provides full-service Phase I-IV clinical trial management, monitoring, regulatory affairs, and data services for global pharmaceutical, biotech, and medical device sponsors, with a specialty in urology and oncology.

What CMX Research does

CMX Research Inc. is a privately held, niche Contract Research Organization headquartered in Oakville, Ontario, Canada. Founded in 1992 as a Site Management Organization, the company has evolved into a full-service CRO providing Phase I–IV clinical trial services for drug and medical device studies, with a stated specialty in urology and oncology. The business is founder-led by Dr. Richard Casey, MD, FRCS(C), an actively practicing urologist and principal investigator, whose clinical background positions CMX around protocol design quality and patient-friendly study execution rather than scale-driven volume.

The company's service portfolio is organized around four core offerings — Full Service CRO (project management, site monitoring, regulatory affairs, vendor procurement, medical writing, safety/medical monitoring, statistical analysis, protocol writing, and eDC data management), Investigator Network (clinical trial sites across Canada and the USA across community, hospital-based, and academic settings), Investigator-Led Trials support, and Monitoring Services (CRA-led SQV/SIV/IMV/COV visits) — supplemented by secondary services such as regulatory submissions to Health Canada and FDA, device trials, recruitment/advertising, and a newly added Pharmacovigilance module launched in 2024. Technology stack is conventional CRO tooling centred on electronic Data Capture (eDC) data management via third-party vendors; no proprietary AI/ML or platform-as-a-service components are disclosed.

CMX generates revenue on a professional-services, project-by-project basis through direct sales engagement with pharmaceutical organizations, biotech firms, and medical device manufacturers. Pricing is custom-tailored per study and not publicly disclosed. Target customers span large global pharma (Pfizer, Novartis, Roche, AstraZeneca, Bayer, Janssen, Lilly, Sanofi, BMS Canada, Amgen, AbbVie, among others), emerging biotech, device companies, and sub-contracted engagements with Tier-1 CROs (IQVIA, PPD, Icon, PRA Health Sciences, Syneos Health, Chiltern). Trials are executed across 13 countries, including Canada, the United States, and multiple European and Asian jurisdictions.

CMX Research firmographics

Firmographics
Name
CMX Research
Legal name
CMX Research Inc.
Website
https://cmxres.com
Company type
Private
Founded year
1992
Operating status
Operating
Headcount range
11–50 employees
Short description
CMX Research Inc. is a privately held, Oakville-based niche Contract Research Organization founded in 1992 that provides full-service Phase I-IV clinical trial management, monitoring, regulatory affairs, and data services for global pharmaceutical, biotech, and medical device sponsors, with a specialty in urology and oncology.
Ownership category
akta.pro rank

CMX Research industry classification

Industry
Product category
Contract Research Organization (CRO) / Clinical Research Services
NAICS
Research and Development in the Physical, Engineering, and Life Sciences (54171), Scientific Research and Development Services (5417)
SIC
Services-Commercial Physical & Biological Research (8731)
akta.pro primary industry
Clinical CROs (Phase I–IV) (HLAGAAAA)
akta.pro secondary industries
Clinical Trial Monitoring Support (On-site/Remote) (HLAGACAG), Clinical Site Start-Up & Activation (Regulatory/Ethics/Contracts) (HLAGACAC), Regulatory Strategy & Global Submissions (IND/CTA/NDA/BLA/MAA) (HLAGAKAA), Specialty Therapeutic-Area CROs (e.g., oncology/rare disease) (HLAGAAAL), Clinical Trial Informatics (EDC/CTMS/eCOA/eTMF) (HLAGAJAM)

Keywords

  • Clinical research services
  • Contract research organization
  • Clinical trial management
  • Pharmacovigilance services
  • Site management organization

Where CMX Research is headquartered

Location

Headquarters

HQ city
Oakville
HQ country
Canada
HQ region
North America

Offices1 record

Markets served

CMX Research business model

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

Revenue model

  1. Clinical Research Services: CMX Research generates revenue through providing full-service CRO services including clinical trial management, monitoring, regulatory affairs, data management, and pharmacovigilance services for Phase I-IV clinical trials. Revenue is earned through service contracts with pharmaceutical companies, biotech firms, and device manufacturers.

Go-to-market motion1 record

Distribution channels1 record

Marketing channels1 record

CMX Research product offering

Product offering

Core offering

CMX Research is a niche Contract Research Organization (CRO) that designs and executes Phase I-IV clinical trials for pharmaceutical, biotech, and medical device sponsors across urology, oncology, immunology, cardiology, dermatology, endocrinology, and respirology. The company delivers full-service clinical trial management including project management, site monitoring and training, regulatory affairs, vendor procurement, medical writing, safety and medical monitoring, statistical analysis, protocol writing, and eDC-based data management. Its services are anchored by the largest urology-oncology principal investigator network in Canada and the USA, and supplemented by recently launched Pharmacovigilance Services.

Product overview

CMX Research is a niche Contract Research Organization (CRO) that evolved from a Site Management Organization (SMO) founded in 1992. Its service portfolio is organized around four interconnected core offerings: Full Service CRO (spanning project management, site monitoring and training, regulatory affairs, vendor procurement, medical writing, safety/medical monitoring, statistical analysis, protocol writing and study design, and eDC data management), Investigator Network (providing access to clinical trial sites across Canada and the USA), Investigator-Led Trials (ILTs) support (covering study design through final report writing), and Monitoring Services (CRA-led visits from SQVs through COVs for Phase I–IV and BA/BE studies). These core services are supplemented by secondary offerings including protocol design, early-phase proof-of-concept studies, regulatory submissions to Health Canada and FDA, device trials, central advertising and recruitment, physician focus groups, and audits. A newly added Pharmacovigilance Services module rounds out the portfolio.

Differentiator

Problem solved

Functional benefit

Products and services

  • Full Service CRO Comprehensive contract research organization services covering Phase I-IV clinical trials for pharmaceutical, biotech, and device sponsors, including project management, site monitoring, regulatory affairs, vendor procurement, medical writing, safety monitoring, statistical analysis, protocol writing, and eDC-based data management.
  • Investigator Network Extensive network of clinical trial sites across Canada and the USA spanning community sites, hospital-based research organizations, and academic institutions, with a focus on urology and oncology principal investigators — described as the largest urology-oncology PI network in North America.
  • Investigator-Led Trials (ILTs) Support services for investigator-initiated trials including study design and launch, study management, site selection and recruitment, budget-friendly pricing and grant support, strategic study support, data management and analysis, and final report writing.
  • Monitoring Services Clinical trial monitoring conducted by trained and certified Clinical Research Associates (CRAs), including Site Qualification Visits (SQVs), Site Initiation Visits (SIVs), Interim Monitoring Visits (IMVs), and Close-Out Visits (COVs) for Phase I-IV and BA/BE studies.
  • Secondary Services Additional services including protocol design and development, early phase / proof of concept studies, regulatory submissions to Health Canada and FDA, device trials, central advertising and recruitment services, call centre support, physician focus groups, and audits.
  • Pharmacovigilance Services Newly launched pharmacovigilance services for safety and adverse event monitoring in clinical trials, extending CMX's service portfolio into post-trial and ongoing safety surveillance.

Quantifiable outcome

  • Completed over 400 studies successfully since 1992
  • +3 more outcomes

Companies that use CMX Research

Customer profile

Named customers33 records

Segments4 records

Ideal customer profiles3 records

CMX Research technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

CMX Research partnerships and signals

Strategic signal

Partnerships

21 partnerships are on record, tiered minor.

  • AB ScienceminorOthersPharmaceutical company listed as a client partner of CMX Research for clinical trial services.
  • AbbVieminorOthersGlobal pharmaceutical company listed as a client partner of CMX Research for clinical trial services.
  • AmgenminorOthersGlobal pharmaceutical company listed as a client partner of CMX Research for clinical trial services.
  • AstraZenecaminorOthersGlobal pharmaceutical company listed as a client partner of CMX Research for clinical trial services.
  • BayerminorOthersGlobal pharmaceutical company listed as a client partner of CMX Research for clinical trial services.
  • Bristol Myers Squibb CanadaminorOthersPharmaceutical company listed as a client partner of CMX Research for clinical trial services.
  • JanssenminorOthersPharmaceutical company (Johnson & Johnson subsidiary) listed as a client partner of CMX Research for clinical trial services.
  • LillyminorOthersGlobal pharmaceutical company listed as a client partner of CMX Research for clinical trial services.
  • NovartisminorOthersGlobal pharmaceutical company listed as a client partner of CMX Research for clinical trial services.
  • PfizerminorOthersGlobal pharmaceutical company listed as a client partner of CMX Research for clinical trial services.
  • RocheminorOthersGlobal pharmaceutical company listed as a client partner of CMX Research for clinical trial services.
  • SanofiminorOthersGlobal pharmaceutical company listed as a client partner of CMX Research for clinical trial services.
  • Boehringer IngelheimminorOthersGlobal pharmaceutical company listed as a client partner of CMX Research for clinical trial services.
  • Daiichi SankyominorOthersGlobal pharmaceutical company listed as a client partner of CMX Research for clinical trial services.
  • Ferring PharmaceuticalsminorOthersPharmaceutical company listed as a client partner of CMX Research for clinical trial services.
  • ChilternminorChannel Partner/ Reseller/ DistributorCMX has worked with Chiltern as a CRO partner, providing clinical trial services.
  • IQVIAminorChannel Partner/ Reseller/ DistributorCMX has collaborated with IQVIA as a CRO partner, providing clinical trial services.
  • IconminorChannel Partner/ Reseller/ DistributorCMX has worked with Icon as a CRO partner, providing clinical trial services.
  • PPDminorChannel Partner/ Reseller/ DistributorCMX has collaborated with PPD as a CRO partner, providing clinical trial services.
  • PRA Health SciencesminorChannel Partner/ Reseller/ DistributorCMX has worked with PRA Health Sciences as a CRO partner, providing clinical trial services.
  • Syneos HealthminorChannel Partner/ Reseller/ DistributorCMX has collaborated with Syneos Health as a CRO partner, providing clinical trial services.

Scale indicators5 records

Recent moves5 records

Expansion highlights5 records

CMX Research competitors and assessment

Company assessment

Emerging players

  • Theorem Clinical Research: Mid-size specialty CRO focused on oncology and complex therapeutics — comparable to CMX on therapeutic specialization and small/mid CRO scale, though with broader geographic footprint.
  • Novum Pharmaceutical Research Services: Niche CRO with early-phase clinical pharmacology and BA/BE expertise — directly comparable to CMX's BA/BE monitoring line and Phase I capability, with similar size and specialty positioning.

Broad incumbents

  • Quintiles (IQVIA): Largest global CRO and a documented CMX channel-partner/sub-contractor. Overlaps with CMX's full-service Phase I-IV offerings but operates at vastly greater scale across all therapeutic areas.
  • Syneos Health / Fortrea: Large clinical and commercial services CRO (post-spin Fortrea) and a documented CMX channel partner — competes across Phase I-IV with broader scale and integrated commercialization.
  • ICON plc: Top-3 global CRO (formed via PRA Health Sciences combination) and a documented CMX channel partner — competing broad CRO with full Phase I-IV capabilities that often sub-contracts site and monitoring work to specialists like CMX.
  • PPD (Thermo Fisher Clinical Research): Top-5 global CRO within Thermo Fisher and a documented CMX channel partner — broad full-service CRO competing with CMX in oncology/urology sponsor work, often leveraging specialists for site execution.

Direct peers

  • Premier Research: Specialty-focused CRO with therapeutic expertise in oncology, urology, rare disease and pediatrics — directly comparable on therapeutic specialization, mid-scale full-service delivery, and PI-relationship-driven model.
  • Medpace: Mid-size, therapeutically-focused full-service CRO with a reputation for medical/scientific depth and investigator-driven execution — directly comparable to CMX's clinical-led, specialty-therapy model, but at substantially greater scale.
  • Worldwide Clinical Trials: Mid-size specialty CRO with strong therapeutic-area depth in oncology, urology and CNS — competes head-to-head with CMX for specialty Phase II/III work and shares the same medical-led positioning.
  • Clinipace Worldwide: Mid-size full-service CRO with oncology and specialty therapeutic expertise and a mix of sponsor and biotech clients — closely comparable on service breadth and therapeutic emphasis.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat4 records

Key risks7 records

Key highlights7 records

Customer concentration

CMX Research social profiles

Digital presence

CMX Research financial estimates

Financial estimate

Revenue estimate

Valuation estimate

CMX Research leadership team

Management profile

Number of profiles

Profiles1 record

CMX Research funding detail

Funding detail

Funding overview

Funding rounds

Investors

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

CMX Research 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 CMX Research

What does CMX Research do?

CMX Research is a niche Contract Research Organization (CRO) that designs and executes Phase I-IV clinical trials for pharmaceutical, biotech, and medical device sponsors across urology, oncology, immunology, cardiology, dermatology, endocrinology, and respirology. The company delivers full-service clinical trial management including project management, site monitoring and training, regulatory affairs, vendor procurement, medical writing, safety and medical monitoring, statistical analysis, protocol writing, and eDC-based data management. Its services are anchored by the largest urology-oncology principal investigator network in Canada and the USA, and supplemented by recently launched Pharmacovigilance Services.

Is CMX Research a public or private company?

CMX Research is a private company. It is classified as founder individual operated bootstrapped and is currently operating.

When was CMX Research founded?

CMX Research was founded in 1992. It employs 11 to 50 people.

Where is CMX Research based?

CMX Research is headquartered in Oakville, Canada, in the North America region.

How does CMX Research make money?

One revenue line is on record: clinical Research Services.

Who are CMX Research's main competitors?

Emerging players on record are Theorem Clinical Research and Novum Pharmaceutical Research Services. Broad incumbents are Quintiles (IQVIA), Syneos Health / Fortrea, ICON plc and PPD (Thermo Fisher Clinical Research). Direct peers are Premier Research, Medpace, Worldwide Clinical Trials and Clinipace Worldwide.

Does CMX Research have an API?

No public API is recorded for CMX Research.

What industry is CMX Research in?

CMX Research's product category is Contract Research Organization (CRO) / Clinical Research Services. Its primary akta.pro industry code is HLAGAAAA, Clinical CROs (Phase I–IV), with a secondary code of HLAGACAG, Clinical Trial Monitoring Support (On-site/Remote). Its NAICS code is 54171 and its SIC code is 8731.

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