Developer docs
API playgroundTry for free, no card

Search company profiles

PHARMExcel

Full company profile

uuid000c7f5

Namestring
PHARMExcel
Legal namestring
PHARMExcel
Company typeenum
Private
Founded yearint
2009
Descriptiontext

PHARMExcel is a privately held UK Contract Research Organisation (CRO) founded in 2009 by Yvanne Enever, headquartered in Welwyn Garden City (with operational roots in Stevenage). The company delivers full-service Phase I-IV clinical research services for both investigational medicinal products and medical devices, spanning 16+ therapeutic areas including hepatology, oncology, haematology, infectious diseases, ophthalmology, gastroenterology, neurology, and rare diseases. Its specialized offerings include ATMP (cell and gene therapy) clinical trials with access to MHRA-licensed facilities, medical device CRO services for Class I-III devices aligned to ISO 14155, rare disease adaptive trial design, and dedicated academic/NHS investigator-initiated study support.

Operationally, PHARMExcel runs an integrated delivery model covering clinical trial development, study/project management, clinical monitoring, regulatory affairs, safety management (SAE/SUSAR reporting and IDMC coordination), data management via 21 CFR Part 11 compliant partner EDC systems, biostatistics (statistical planning, TLF generation, DSMB outputs), and quality/compliance (audits, CAPA, regulatory inspection support). The company operates an ISO 9001:2015 certified Quality Management System and uses risk-based monitoring methodologies. Technology infrastructure is largely partner-provided rather than proprietary, with no disclosed AI/ML capabilities.

Commercially, PHARMExcel employs a 'pick and mix' professional services pricing model allowing sponsors to procure individual services or full-service bundles on multi-year contracts with itemised costings. The go-to-market is sales-led and direct, targeting NHS Trusts, universities, Clinical Trials Units, biotech start-ups and university spin-outs, medical device companies, and rare disease sponsors. The company is founder-led, self-funded with no disclosed external equity or debt rounds, and operates as PHARMExcel Ltd (UK private limited company) with a team of 11-50 employees. Notable customer relationships include UCL, Imperial College London, Moorfields Eye Hospital, University Hospital Southampton, INmune Bio, Axovia Therapeutics, Sequana Medical, and Yaqrit, supported by partnerships with the ECMC Network, UK Biomedical Research Centres, Clinical Research Facilities, Cancer Research Networks, and patient advocacy groups such as the MPS Society and Beacon for Rare Diseases.

Short descriptiontext

PHARMExcel is a UK-based full-service CRO providing Phase I-IV clinical research services for drug and medical device studies. Founded in 2009, the company serves NHS trusts, universities, biotechs, and medical device manufacturers, specializing in ATMP, early-phase, and rare disease trials.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersStevenage, United Kingdom
HQ citystring
Stevenage
HQ countrystring
United Kingdom
HQ regionstring
Europe
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, regulatory affairs services, biostatistics data management
Industry3 codes
1Specialty Therapeutic-Area CROs (e.g., oncology/rare disease)
CodeHLAGAAALPrimaryNo
2Patient Recruitment, Site Feasibility & Trial Enablement CROs
CodeHLAGAAAIPrimaryNo
3Medical Writing & Regulatory Submission Support CROs
CodeHLAGAAAGPrimaryNo
NAICS code2 codes
  • Scientific Research and Development Services5417
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
SIC code1 code
  • Services-Commercial Physical & Biological Research8731
Product category
Contract Research Services
Social media profiles2 records
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model1 record
1Clinical Research Services
TypeProfessional Services
Description

PHARMExcel provides comprehensive CRO services including clinical trial development, management, monitoring, regulatory affairs, data management, biostatistics, safety management, and quality compliance. Services can be selected à la carte ('pick and mix' model) or as full-service delivery.

pharmexcel-cro.com
Marketing channels7 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, Operations, Technology or R&D, Marketing or Sales, Others
Pricing details1 tier
1Flexible service model - clients select specific services as needed
ModelOtherBilling cadenceMulti-year contract
Notes

Flexible 'pick and mix' model allowing sponsors to engage specific services tailored to each project requirements. Detailed, itemised costings provide full visibility over budget and deliverables.

pharmexcel-cro.com
GTM typeB2B
B2B
Offering typeServices
Services
Core offering1 text field

PHARMExcel is a UK-based full-service Contract Research Organisation (CRO) providing Phase I-IV clinical research services to the NHS, Universities, Biopharma and Medical Device sectors. It delivers flexible, integrated clinical trial development, management, monitoring, regulatory affairs, data management, biostatistics, safety management, and quality compliance services through a 'pick and mix' model. Specialized offerings include ATMP (cell/gene therapy), medical device, rare disease, biotech, and academic/NHS trial support.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 2 values shown
  • 70% PTSR (Probability of Technical and Regulatory Success) indication benchmark achieved for progressing INKmune programme into Phase II
+1 more record
Product overview1 text field

PHARMExcel is a full-service Contract Research Organisation (CRO) providing Phase I-IV clinical research services through a flexible, integrated delivery model. The company operates as a single unified offering with a 'mix-and-match' service architecture, allowing sponsors to engage specific services tailored to each project. Core services include Clinical Trial Development, Study/Project Management, Clinical Monitoring, Regulatory Affairs, Safety Management, Data Management (powered by 21 CFR Part 11 compliant EDC systems), Biostatistics, and Quality and Compliance. Specialized offerings span Academic/NHS/University Trials, Biotech CRO Services, ATMP Clinical Trials, Medical Device CRO Services, and Rare Disease Clinical Trials. The company delivers across 16+ therapeutic areas including Oncology/Haematology, Hepatology, Infectious Diseases/Vaccines, Ophthalmology, Neurology, Cardiovascular, Gastroenterology, and Rare Diseases, with geographic reach across UK, EU, and USA sites.

Product and service15 records
1Phase I Clinical Trial Services
CategoryClinical Trial Management
Description

Early-phase clinical trial services covering first-in-human and first-in-patient studies, with particular expertise in ATMP, rare disease, oncology, haematology and ophthalmology, leveraging UK regulatory knowledge and MHRA-licensed facilities.

2Phase II-IV Clinical Trial Services
CategoryClinical Trial Management
Description

Mid-to-late phase clinical trial delivery spanning Phase II, III and IV studies across broad therapeutic areas, supporting both IMP and medical device investigations.

3Clinical Trial Development
CategoryClinical Trial Management
Description

Comprehensive clinical trial development services including protocol development, patient-facing documents (patient information sheets, informed consent forms), and clinical study reports aligned to ICH E3 or ISO standards.

4Study and Project Management
CategoryClinical Trial Management
Description

End-to-end study and project management services coordinating all aspects of clinical trial delivery from start-up through to monitoring and close-out.

5Clinical Monitoring
CategoryClinical Trial Management
Description

GCP-trained CRA monitoring services ensuring compliance with regulatory requirements across UK and EU sites.

6Regulatory Affairs
CategoryRegulatory Affairs
Description

Preparation and management of clinical trial applications, substantial amendments and end of trial notifications to UK and EU Competent Authorities including MHRA.

7Safety Management
CategoryClinical Trial Management
Description

Comprehensive safety management including protocol safety section development, SAE/SADE processing, SUSAR/USADE expedited reporting, safety monitoring plans and independent drug safety monitoring committee (IDMC) management.

8Data Management
CategoryData Management
Description

Electronic data capture solutions with 21 CFR Part 11 compliant software, visit scheduling, real-time edit checks, automated query management, and integration with GlobalTrace EDC for kit tracking.

9Biostatistics
CategoryBiostatistics
Description

Statistical planning, innovative study design, randomisation schedules, submission-ready datasets, TLF generation, DSMB outputs, interim analysis support, and manuscript/abstract statistical support.

10Quality and Compliance
CategoryQuality Assurance
Description

Quality management plans, clinical quality assurance services including investigator site audits, document reviews, system audits, vendor audits, and regulatory inspection support with CAPA development.

11Academic and NHS University Trials Services
CategorySpecialized CRO Services
Description

Bespoke CRO services supporting NHS trusts, universities, Clinical Trials Units and spin-outs with pre-funding guidance, protocol development, regulatory approvals, and flexible 'pick and mix' service delivery.

12Biotech CRO Services
CategorySpecialized CRO Services
Description

Specialized clinical trial support for biotechs and university spin-outs, offering Phase I-II expertise, ATMP and rare disease study capabilities, medical device studies, rescue studies, and flexible cost-transparent service models.

13ATMP Clinical Trial Services
CategorySpecialized CRO Services
Description

Advanced Therapy Medicinal Product clinical trial services for cell and gene therapies, including first-in-human and first-in-patient studies with Phase I fast-track approvals, product traceability, and access to MHRA-licensed facilities and apheresis sites.

14Medical Device CRO Services
CategorySpecialized CRO Services
Description

Full-service medical device and diagnostics CRO supporting Class I-III device studies through ISO 14155-compliant clinical investigations, UKCA and CE marking evidence generation, and combination product trials.

15Rare Disease Clinical Trial Services
CategorySpecialized CRO Services
Description

Specialized rare disease trial services featuring adaptive trial design, patient advocacy group partnerships, multi-site setup, and expedited regulatory approvals across multiple therapeutic indications.

Scale indicator4 records

Each record includes

Type, Value, Description, Source

Partnership8 partners
Strategic tierCoreTypeStrategic or Co-development Partner
Description

PHARMExcel partners with Rare Disease Research Partners to provide enhanced trial design for sponsors, patients, and sites in Fabry disease and MPS clinical trials. The collaboration combines PHARMExcel's CRO expertise with research partner capabilities.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

PHARMExcel sponsors the Fabry Matters Research Grant in partnership with MPS Society, supporting rare disease research and patient communities. This collaboration enhances trial experiences and accelerates delivery of novel therapies.

3Beacon for Rare Diseases
Strategic tierMinorTypeStrategic or Co-development Partner
Description

PHARMExcel supports Beacon for Rare Diseases as their chosen charity of the year, participating in fundraising activities and community support initiatives.

pharmexcel-cro.com
Strategic tierCoreTypeStrategic or Co-development Partner
Description

PHARMExcel collaborates with the ECMC Network to deliver complex oncology trials including the Phase I TRALA trial for AL Amyloidosis treatment. ECMC provides clinical infrastructure and specialist capabilities for early-phase cancer research.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

PHARMExcel has established partnerships with UK Biomedical Research Centres providing access to specialist research sites and centres of excellence for rare disease clinical trials.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

PHARMExcel works with Clinical Research Facilities across the UK to deliver early-phase clinical trials with access to specialized infrastructure and clinical expertise.

Strategic tierCoreTypeChannel Partner/ Reseller/ Distributor
Description

PHARMExcel leverages Cancer Networks across the UK for oncology clinical trial delivery, enabling access to a wide network of research sites and investigators.

Strategic tierCoreTypeChannel Partner/ Reseller/ Distributor
Description

PHARMExcel utilizes Clinical Research Networks to access NHS sites and coordinate multi-site trial delivery across the UK healthcare system.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Global early-phase clinical CRO specialising in first-in-human, biopharmaceutics and PK/PD studies. Comparable to PHARMExcel on early-phase focus and ATMP/experimental medicine capability, though at much larger scale.

TypeBroad incumbent
Description

Mid-size global full-service CRO with strong biotech sponsor franchise across all phases. Comparable in offering Phase I-IV clinical services to biotech/specialty pharma, but at materially larger scale and broader geographic reach than PHARMExcel.

TypeBroad incumbent
Description

Global full-service CRO with biotech/specialty pharma franchise. Comparable on full-service Phase I-IV clinical delivery, though at significantly larger scale and broader therapeutic coverage than PHARMExcel.

TypeBroad incumbent
Description

World's largest CRO with full Phase I-IV capabilities, technology platforms and global reach. Comparable to PHARMExcel across the clinical trial service stack, but as a broad incumbent offering PHARMExcel's specialist services as part of a much wider portfolio.

TypeEmerging player
Description

Mid-size global CRO focused on biotech and specialty pharma across rare disease, oncology and CNS. Comparable to PHARMExcel on biotech-centric, mid-size full-service clinical delivery model; competing for similar sponsor relationships.

TypeDirect peer
Description

UK-origin specialist CRO with strong orphan/rare disease and oncology focus before its acquisition. Highly comparable to PHARMExcel on UK base, rare disease/oncology specialism, and mid-size CRO profile targeting biotech and academic sponsors.

TypeDirect peer
Description

Mid-sized global CRO offering clinical trial management alongside bioanalytical and lab services. Comparable on clinical CRO services for biotech and specialty pharma; overlaps with PHARMExcel on full-service Phase I-IV delivery model.

TypeBroad incumbent
Description

Mid-size global CRO with strong rare disease, CNS and specialty therapeutic focus. Comparable on Phase I-IV clinical delivery and rare disease expertise, though substantially larger and more geographically diverse than PHARMExcel.

TypeDirect peer
Description

UK specialist CRO/clinical research unit focused on early-phase trials including ATMP and vaccine studies. Comparable to PHARMExcel on Phase I specialism, UK base and investigator/sponsor crossover work.

TypeDirect peer
Description

UK-based early-phase clinical research unit and specialist CRO with strong MHRA Phase I expertise. Directly comparable to PHARMExcel on Phase I/early-phase focus, UK regulatory specialism and academic/NHS client base; competes for similar ATMP and first-in-human sponsors.

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

Customer concentration

Classification, Details

Named customers13 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 profile4 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

Feature3 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles15 records

Each record includes

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

No data
Compliance1 record

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 →

PHARMExcel

Contract Research Servicespharmexcel-cro.com

PHARMExcel is a UK-based full-service CRO providing Phase I-IV clinical research services for drug and medical device studies. Founded in 2009, the company serves NHS trusts, universities, biotechs, and medical device manufacturers, specializing in ATMP, early-phase, and rare disease trials.

What PHARMExcel does

PHARMExcel is a privately held UK Contract Research Organisation (CRO) founded in 2009 by Yvanne Enever, headquartered in Welwyn Garden City (with operational roots in Stevenage). The company delivers full-service Phase I-IV clinical research services for both investigational medicinal products and medical devices, spanning 16+ therapeutic areas including hepatology, oncology, haematology, infectious diseases, ophthalmology, gastroenterology, neurology, and rare diseases. Its specialized offerings include ATMP (cell and gene therapy) clinical trials with access to MHRA-licensed facilities, medical device CRO services for Class I-III devices aligned to ISO 14155, rare disease adaptive trial design, and dedicated academic/NHS investigator-initiated study support.

Operationally, PHARMExcel runs an integrated delivery model covering clinical trial development, study/project management, clinical monitoring, regulatory affairs, safety management (SAE/SUSAR reporting and IDMC coordination), data management via 21 CFR Part 11 compliant partner EDC systems, biostatistics (statistical planning, TLF generation, DSMB outputs), and quality/compliance (audits, CAPA, regulatory inspection support). The company operates an ISO 9001:2015 certified Quality Management System and uses risk-based monitoring methodologies. Technology infrastructure is largely partner-provided rather than proprietary, with no disclosed AI/ML capabilities.

Commercially, PHARMExcel employs a 'pick and mix' professional services pricing model allowing sponsors to procure individual services or full-service bundles on multi-year contracts with itemised costings. The go-to-market is sales-led and direct, targeting NHS Trusts, universities, Clinical Trials Units, biotech start-ups and university spin-outs, medical device companies, and rare disease sponsors. The company is founder-led, self-funded with no disclosed external equity or debt rounds, and operates as PHARMExcel Ltd (UK private limited company) with a team of 11-50 employees. Notable customer relationships include UCL, Imperial College London, Moorfields Eye Hospital, University Hospital Southampton, INmune Bio, Axovia Therapeutics, Sequana Medical, and Yaqrit, supported by partnerships with the ECMC Network, UK Biomedical Research Centres, Clinical Research Facilities, Cancer Research Networks, and patient advocacy groups such as the MPS Society and Beacon for Rare Diseases.

PHARMExcel firmographics

Firmographics
Name
PHARMExcel
Legal name
PHARMExcel
Website
https://pharmexcel-cro.com
Company type
Private
Founded year
2009
Operating status
Operating
Headcount range
11–50 employees
Short description
PHARMExcel is a UK-based full-service CRO providing Phase I-IV clinical research services for drug and medical device studies. Founded in 2009, the company serves NHS trusts, universities, biotechs, and medical device manufacturers, specializing in ATMP, early-phase, and rare disease trials.
Ownership category
akta.pro rank

Where PHARMExcel is headquartered

Location

Headquarters

HQ city
Stevenage
HQ country
United Kingdom
HQ region
Europe

Offices1 record

Markets served

PHARMExcel business model

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

Revenue model

  1. Clinical Research Services: PHARMExcel provides comprehensive CRO services including clinical trial development, management, monitoring, regulatory affairs, data management, biostatistics, safety management, and quality compliance. Services can be selected à la carte ('pick and mix' model) or as full-service delivery.

Pricing tiers

ModelBillingPrice
OtherMulti-year contractFlexible service model - clients select specific services as needed

Go-to-market motion1 record

Distribution channels1 record

Marketing channels7 records

PHARMExcel product offering

Product offering

Core offering

PHARMExcel is a UK-based full-service Contract Research Organisation (CRO) providing Phase I-IV clinical research services to the NHS, Universities, Biopharma and Medical Device sectors. It delivers flexible, integrated clinical trial development, management, monitoring, regulatory affairs, data management, biostatistics, safety management, and quality compliance services through a 'pick and mix' model. Specialized offerings include ATMP (cell/gene therapy), medical device, rare disease, biotech, and academic/NHS trial support.

Product overview

PHARMExcel is a full-service Contract Research Organisation (CRO) providing Phase I-IV clinical research services through a flexible, integrated delivery model. The company operates as a single unified offering with a 'mix-and-match' service architecture, allowing sponsors to engage specific services tailored to each project. Core services include Clinical Trial Development, Study/Project Management, Clinical Monitoring, Regulatory Affairs, Safety Management, Data Management (powered by 21 CFR Part 11 compliant EDC systems), Biostatistics, and Quality and Compliance. Specialized offerings span Academic/NHS/University Trials, Biotech CRO Services, ATMP Clinical Trials, Medical Device CRO Services, and Rare Disease Clinical Trials. The company delivers across 16+ therapeutic areas including Oncology/Haematology, Hepatology, Infectious Diseases/Vaccines, Ophthalmology, Neurology, Cardiovascular, Gastroenterology, and Rare Diseases, with geographic reach across UK, EU, and USA sites.

Differentiator

Problem solved

Functional benefit

Products and services

  • Phase I Clinical Trial Services Early-phase clinical trial services covering first-in-human and first-in-patient studies, with particular expertise in ATMP, rare disease, oncology, haematology and ophthalmology, leveraging UK regulatory knowledge and MHRA-licensed facilities.
  • Phase II-IV Clinical Trial Services Mid-to-late phase clinical trial delivery spanning Phase II, III and IV studies across broad therapeutic areas, supporting both IMP and medical device investigations.
  • Clinical Trial Development Comprehensive clinical trial development services including protocol development, patient-facing documents (patient information sheets, informed consent forms), and clinical study reports aligned to ICH E3 or ISO standards.
  • Study and Project Management End-to-end study and project management services coordinating all aspects of clinical trial delivery from start-up through to monitoring and close-out.
  • Clinical Monitoring GCP-trained CRA monitoring services ensuring compliance with regulatory requirements across UK and EU sites.
  • Regulatory Affairs Preparation and management of clinical trial applications, substantial amendments and end of trial notifications to UK and EU Competent Authorities including MHRA.
  • Safety Management Comprehensive safety management including protocol safety section development, SAE/SADE processing, SUSAR/USADE expedited reporting, safety monitoring plans and independent drug safety monitoring committee (IDMC) management.
  • Data Management Electronic data capture solutions with 21 CFR Part 11 compliant software, visit scheduling, real-time edit checks, automated query management, and integration with GlobalTrace EDC for kit tracking.
  • Biostatistics Statistical planning, innovative study design, randomisation schedules, submission-ready datasets, TLF generation, DSMB outputs, interim analysis support, and manuscript/abstract statistical support.
  • Quality and Compliance Quality management plans, clinical quality assurance services including investigator site audits, document reviews, system audits, vendor audits, and regulatory inspection support with CAPA development.
  • Academic and NHS University Trials Services Bespoke CRO services supporting NHS trusts, universities, Clinical Trials Units and spin-outs with pre-funding guidance, protocol development, regulatory approvals, and flexible 'pick and mix' service delivery.
  • Biotech CRO Services Specialized clinical trial support for biotechs and university spin-outs, offering Phase I-II expertise, ATMP and rare disease study capabilities, medical device studies, rescue studies, and flexible cost-transparent service models.
  • ATMP Clinical Trial Services Advanced Therapy Medicinal Product clinical trial services for cell and gene therapies, including first-in-human and first-in-patient studies with Phase I fast-track approvals, product traceability, and access to MHRA-licensed facilities and apheresis sites.
  • Medical Device CRO Services Full-service medical device and diagnostics CRO supporting Class I-III device studies through ISO 14155-compliant clinical investigations, UKCA and CE marking evidence generation, and combination product trials.
  • Rare Disease Clinical Trial Services Specialized rare disease trial services featuring adaptive trial design, patient advocacy group partnerships, multi-site setup, and expedited regulatory approvals across multiple therapeutic indications.

Quantifiable outcome

  • 70% PTSR (Probability of Technical and Regulatory Success) indication benchmark achieved for progressing INKmune programme into Phase II
  • +1 more outcomes

Companies that use PHARMExcel

Customer profile

Named customers13 records

Segments4 records

Ideal customer profiles4 records

PHARMExcel technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature3 records

PHARMExcel partnerships and signals

Strategic signal

Partnerships

Eight partnerships are on record, tiered core and minor.

  • Rare Disease Research PartnerscoreStrategic or Co-development PartnerPHARMExcel partners with Rare Disease Research Partners to provide enhanced trial design for sponsors, patients, and sites in Fabry disease and MPS clinical trials. The collaboration combines PHARMExcel's CRO expertise with research partner capabilities.
  • MPS SocietycoreStrategic or Co-development PartnerPHARMExcel sponsors the Fabry Matters Research Grant in partnership with MPS Society, supporting rare disease research and patient communities. This collaboration enhances trial experiences and accelerates delivery of novel therapies.
  • Beacon for Rare DiseasesminorStrategic or Co-development PartnerPHARMExcel supports Beacon for Rare Diseases as their chosen charity of the year, participating in fundraising activities and community support initiatives.
  • Experimental Cancer Medicine Centre (ECMC) NetworkcoreStrategic or Co-development PartnerPHARMExcel collaborates with the ECMC Network to deliver complex oncology trials including the Phase I TRALA trial for AL Amyloidosis treatment. ECMC provides clinical infrastructure and specialist capabilities for early-phase cancer research.
  • UK Biomedical Research Centres (BRCs)coreStrategic or Co-development PartnerPHARMExcel has established partnerships with UK Biomedical Research Centres providing access to specialist research sites and centres of excellence for rare disease clinical trials.
  • UK Clinical Research Facilities (CRFs)coreStrategic or Co-development PartnerPHARMExcel works with Clinical Research Facilities across the UK to deliver early-phase clinical trials with access to specialized infrastructure and clinical expertise.
  • Cancer Research NetworkscoreChannel Partner/ Reseller/ DistributorPHARMExcel leverages Cancer Networks across the UK for oncology clinical trial delivery, enabling access to a wide network of research sites and investigators.
  • UK Clinical Research NetworkscoreChannel Partner/ Reseller/ DistributorPHARMExcel utilizes Clinical Research Networks to access NHS sites and coordinate multi-site trial delivery across the UK healthcare system.

Scale indicators4 records

Recent moves6 records

Expansion highlights6 records

PHARMExcel competitors and assessment

Company assessment

Direct peers

  • Celerion: Global early-phase clinical CRO specialising in first-in-human, biopharmaceutics and PK/PD studies. Comparable to PHARMExcel on early-phase focus and ATMP/experimental medicine capability, though at much larger scale.
  • Ergomed (now part of Asymchem): UK-origin specialist CRO with strong orphan/rare disease and oncology focus before its acquisition. Highly comparable to PHARMExcel on UK base, rare disease/oncology specialism, and mid-size CRO profile targeting biotech and academic sponsors.
  • Frontage Laboratories: Mid-sized global CRO offering clinical trial management alongside bioanalytical and lab services. Comparable on clinical CRO services for biotech and specialty pharma; overlaps with PHARMExcel on full-service Phase I-IV delivery model.
  • Hammersmith Medicines Research: UK specialist CRO/clinical research unit focused on early-phase trials including ATMP and vaccine studies. Comparable to PHARMExcel on Phase I specialism, UK base and investigator/sponsor crossover work.
  • Richmond Pharmacology: UK-based early-phase clinical research unit and specialist CRO with strong MHRA Phase I expertise. Directly comparable to PHARMExcel on Phase I/early-phase focus, UK regulatory specialism and academic/NHS client base; competes for similar ATMP and first-in-human sponsors.

Broad incumbents

  • Medpace: Mid-size global full-service CRO with strong biotech sponsor franchise across all phases. Comparable in offering Phase I-IV clinical services to biotech/specialty pharma, but at materially larger scale and broader geographic reach than PHARMExcel.
  • ICON plc: Global full-service CRO with biotech/specialty pharma franchise. Comparable on full-service Phase I-IV clinical delivery, though at significantly larger scale and broader therapeutic coverage than PHARMExcel.
  • IQVIA: World's largest CRO with full Phase I-IV capabilities, technology platforms and global reach. Comparable to PHARMExcel across the clinical trial service stack, but as a broad incumbent offering PHARMExcel's specialist services as part of a much wider portfolio.
  • Worldwide Clinical Trials: Mid-size global CRO with strong rare disease, CNS and specialty therapeutic focus. Comparable on Phase I-IV clinical delivery and rare disease expertise, though substantially larger and more geographically diverse than PHARMExcel.

Emerging players

  • Biorasi: Mid-size global CRO focused on biotech and specialty pharma across rare disease, oncology and CNS. Comparable to PHARMExcel on biotech-centric, mid-size full-service clinical delivery model; competing for similar sponsor relationships.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat4 records

Customer concentration

PHARMExcel social profiles

Digital presence

PHARMExcel compliance and trust

Trust signal

Compliance1 record

PHARMExcel financial estimates

Financial estimate

Revenue estimate

Valuation estimate

PHARMExcel leadership team

Management profile

Number of profiles

Profiles15 records

PHARMExcel funding detail

Funding detail

Funding overview

Funding rounds

Investors

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

PHARMExcel 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 PHARMExcel

What does PHARMExcel do?

PHARMExcel is a UK-based full-service Contract Research Organisation (CRO) providing Phase I-IV clinical research services to the NHS, Universities, Biopharma and Medical Device sectors. It delivers flexible, integrated clinical trial development, management, monitoring, regulatory affairs, data management, biostatistics, safety management, and quality compliance services through a 'pick and mix' model. Specialized offerings include ATMP (cell/gene therapy), medical device, rare disease, biotech, and academic/NHS trial support.

Is PHARMExcel a public or private company?

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

When was PHARMExcel founded?

PHARMExcel was founded in 2009. It employs 11 to 50 people.

Where is PHARMExcel based?

PHARMExcel is headquartered in Stevenage, United Kingdom, in the Europe region.

How does PHARMExcel make money?

One revenue line is on record: clinical Research Services.

Who are PHARMExcel's main competitors?

Direct peers on record are Celerion, Ergomed (now part of Asymchem), Frontage Laboratories, Hammersmith Medicines Research and Richmond Pharmacology. Broad incumbents are Medpace, ICON plc, IQVIA and Worldwide Clinical Trials. Biorasi is listed as an emerging player.

Does PHARMExcel have an API?

No public API is recorded for PHARMExcel.

Unlock the full company data

50 free credits on sign-up, no credit card required.

Contact sales
Live signals