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Clean Cells

Full company profile

uuid000d378

Namestring
Clean Cells
Legal namestring
Clean Cells
Company typeenum
Private
Founded yearint
2000
Descriptiontext

Clean Cells is a France-headquartered biopharmaceutical CMO/CRO founded in 2000, specializing in cGMP-compliant manufacturing of cell and virus banks and quality control testing for biologics including vaccines, therapeutic proteins, gene therapies, and cell therapies. The company operates from a 5,300 m2 facility in Montaigu-Vendée (near Nantes) with 9 GMP production suites and BSL2/BSL3 laboratory capabilities, and supports clients in North America through subsidiaries KaryoLogic (acquired April 2025) and Stem Genomics (acquired June 2026). Its service portfolio covers the full product lifecycle from cell banking, virus seed stock production, and clonal selection through biosafety testing, product characterization, lot release testing, and secure long-term storage, with 250+ validated assays across potency, identity, purity, and biosafety dimensions.

The company serves 230+ biopharmaceutical customers worldwide, performing 7,000+ analyses annually, and holds a granted patent on a non-radioactive luminescent potency assay for cytolytic activity (extended to Europe and Canada). Clean Cells generates revenue through professional services contracts on a quote-based, B2B basis, with an enterprise field sales motion supported by participation in major industry conferences (BIO-Europe, ESACT, ESGCT, CPHI) and educational webinars. The business is part of the Clean Biologics group backed by healthcare-focused private equity firm ArchiMed (majority shareholder since October 2018), alongside sister company Naobios (viral vaccine CDMO acquired March 2019). Following the 2023 facility expansion and recent US-focused acquisitions, Clean Cells is positioned as one of the largest European providers of biopharmaceutical QC services and cell bank production, with 127-133 employees as of the most recent reporting.

Short descriptiontext

Clean Cells is a French CMO/CRO providing cGMP-compliant cell and virus bank manufacturing and biopharmaceutical quality control testing for vaccines, proteins, gene therapies, and cell therapies, serving 230+ global biopharma customers from its 5,300 m2 Montaigu-Vendée facility and US subsidiaries.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
101–250
akta.pro rankint
HeadquartersBoufféré, France
HQ citystring
Boufféré
HQ countrystring
France
HQ regionstring
Europe
Markets served

Serves global market

Offices3 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
biologics testing services, cell bank manufacturing, virus bank manufacturing, biosafety testing services, pharmaceutical quality control
Industry6 codes
1Analytical Development & QC Testing (Release/Stability/Potency)
CodeHLAGAGAFPrimaryYes
2Gene Therapy Analytical Testing & QC (potency, vg/ddPCR, infectivity, RCL/RCA)
CodeHLAAACAKPrimaryNo
3Cell Therapy Quality, Analytics & Release Testing (potency, sterility, comparability)
CodeHLAAABAKPrimaryNo
4Cell Therapy Manufacturing Services (GMP, autologous/allogeneic)
CodeHLAAAKACPrimaryNo
5GMP Manufacturing Support Services (QA/QMS, validation, documentation)
CodeHLAAAKAHPrimaryNo
6Environmental Monitoring & Cleanroom Testing (GMP)
CodeHLAGADALPrimaryNo
NAICS code3 codes
  • Medical Laboratories621511
  • Medical and Diagnostic Laboratories6215
  • Medical and Diagnostic Laboratories62151
SIC code3 codes
  • Services-Medical Laboratories8071
  • Biological Products, (No Disgnostic Substances)2836
  • Services-Testing Laboratories8734
Product category
Biopharmaceutical Quality Control Services
GTM motion3 records

Each record includes

Type, Description, Source

Revenue model4 records
1Quality Control and Biosafety Testing Services
TypeProfessional Services
Description

The company provides biological safety tests and quality control testing for biopharmaceutical products to assist in regulatory compliance. Services include biosafety testing, product characterization, raw material testing, cell bank testing, virus bank testing, and lot release testing.

clean-cells.com
2Cell and Virus Bank Manufacturing
TypeProfessional Services
Description

Production of cell banks and GMP-grade BSL2/BSL3 virus seed stock for use as starting materials in biopharmaceutical manufacturing. Services include clonal selection, cell banking, and virus banking.

clean-cells.com
3Biologics Storage Services
TypeManaged Services
Description

Secure storage services for cell banks and virus banks with options for shared or dedicated containers, continuous temperature monitoring, and backup systems.

clean-cells.com
4Analytical Development
TypeProfessional Services
Description

Development and validation of bespoke analysis tools for biopharmaceutical products, including custom assay development.

clean-cells.com
Marketing channels5 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components6 values
Personnel, Infrastructure, Operations, Technology or R&D, Marketing or Sales, Supply Chain
GTM typeB2B
B2B
Offering typeServices
Services
Core offering1 text field

Clean Cells is a CMO/CRO providing GMP-compliant cell and virus bank manufacturing together with comprehensive quality control testing services for biopharmaceutical products. Its offering covers biosafety testing, product characterization, cell and virus bank testing, lot release testing, raw material testing, analytical development, and secure long-term storage, supporting vaccine, therapeutic protein, gene therapy, cell therapy, and ATMP developers from R&D through market release in compliance with worldwide regulatory agencies.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 4 values shown
  • 5,300 m2 facility quadruples analysis and production capacity
+3 more records
Product overview1 text field

Clean Cells operates as a comprehensive CMO/CRO providing integrated services for the biologics and biopharmaceutical industry. The core offering combines biologics biomanufacturing (cell banking, virus banking, clonal selection) with extensive biologics testing services (biosafety testing, product characterization, cell/virus bank testing, lot release testing, raw material testing). Additional services include analytical development, long-term storage solutions for cell and virus banks, phage therapy CDMO services, and viral safety testing for gene therapy products. The portfolio is complemented by the 2026 acquisition of Stem Genomics' iCS-digital PSC technology for stem cell genomic stability testing. Clean Cells serves global customers from facilities in France with US operations through subsidiaries KaryoLogic and Stem Genomics, offering a one-stop-shop solution from R&D through market release under GMP compliance.

Product and service13 records
1Biologics Biomanufacturing Services
CategoryBiologics Biomanufacturing
Description

Comprehensive manufacturing services for cell banks, virus banks, and clonal selection, including production of GMP or non-GMP Master and Working cell banks, virus seed stock manufacturing under BSL2/BSL3 conditions, and end of production cells generation for biopharmaceutical developers.

2Biosafety Testing
CategoryBiologics Testing
Description

Comprehensive biosafety testing services including microbiology testing (sterility, mycoplasma, endotoxin), viral safety testing, and adventitious agent detection to ensure biological product safety and regulatory compliance for biopharmaceutical developers.

3Product Characterization
CategoryBiologics Testing
Description

Full characterization services for biologics including impurity testing, potency testing (ADCC/CDC/cell-based assays including the patented cytolytic activity assay), and biologics identity testing, supporting regulatory compliance from R&D through market release.

4Cell Bank Testing
CategoryBiologics Testing
Description

Comprehensive testing services for cell banks including sterility, mycoplasma, mycobacteria, adventitious agent detection (in-vivo, in-vitro), specific pathogen testing, retrovirus detection (electron microscopy, infectivity assays, qPERT), identity testing, and genetic stability assessment.

5Virus Bank Testing
CategoryBiologics Testing
Description

Complete virus bank characterization services in GMP conditions ensuring safety, potency, and reliability, including comprehensive viral detection by qPCR covering more than 250 viruses.

6Lot Release Testing
CategoryBiologics Testing
Description

Quality control testing services for lot release of biological products, ensuring product safety, identity, purity, and potency meet regulatory requirements before commercial distribution.

7Raw Material Testing
CategoryBiologics Testing
Description

Testing services for raw materials used in biopharmaceutical manufacturing, ensuring quality and safety of starting materials and reagents.

8Cell Bank Storage
CategoryBiologics Storage
Description

Long-term secure storage services for cell banks at ultra-low temperatures (below -145°C) using liquid or vapor-phase nitrogen tanks or ultra-low temperature freezers, with dedicated or shared container options and continuous temperature monitoring.

9Virus Bank Storage
CategoryBiologics Storage
Description

Secure long-term storage for virus banks at temperatures as low as -80°C, including shared container storage with dedicated boxes or shelves, continuous temperature monitoring, externalized alarm systems, and backup freezer for added security.

10Analytical Development
CategoryAnalytical Development
Description

Custom assay development and validation services for biopharmaceutical products in GMP and non-GMP settings, including implementation of innovative techniques such as digital PCR (dPCR) for quantification of nucleic acids.

11Phage Therapy CDMO Services
CategoryContract Manufacturing
Description

Contract development and manufacturing services for therapeutic bacteriophages, including process development, GMP manufacturing, and purification services for phage therapy products.

12Viral Safety Testing for Gene Therapy
CategoryBiologics Testing
Description

Comprehensive GMP biosafety testing services for gene therapy products including recombinant lentiviral vectors (rLv), with detection of replication-competent lentiviral particles (RCL), and potency and safety characterization for ATMPs.

13Stem Genomics iCS-digital PSC Genomic Stability Testing
CategoryBiologics Testing
Description

Next-generation genomic stability quality controls for human pluripotent stem cells (hPSCs) using the iCS-digital PSC technology platform, addressing genomic integrity requirements for advanced cell therapy developers.

Scale indicator11 records

Each record includes

Type, Value, Description, Source

Partnership8 partners
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-06-18
Description

Acquired in June 2026 to strengthen cell therapy quality control and expand US presence. Provider of next-generation quality controls for stem cell therapy including iCS-digital PSC technology platform. Works with 150+ clients worldwide including academic institutions, biotech companies, and core facilities. Operations in Montpellier, France and Durham, North Carolina.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2025-04-01
Description

Acquired to accelerate expansion in US biologics market. US subsidiary of Clean Cells located in Durham, North Carolina, providing services to North American clients.

Strategic tierMinorTypeStrategic or Co-development Partner
Description

Collaborative partner in HybridADCC project, a €2.4M funded initiative developing standardised ADCC assay for testing mouse monoclonal antibodies using hybrid human/mouse technology.

Strategic tierMinorTypeStrategic or Co-development Partner
Description

Research partner in HybridADCC collaborative project focused on developing standardised ADCC assay methodology for therapeutic antibody characterization.

5MicroPiCell platform
Strategic tierMinorTypeStrategic or Co-development Partner
Description

Academic platform partner in HybridADCC project providing expertise in cell technology for antibody development.

clean-cells.com
6France Biolead
Strategic tierMinorTypeOthers
Description

Founding member of France Biolead association supporting the production of biological medicines alongside major actors such as Sanofi, Servier, INSERM, CEA.

clean-cells.com
Strategic tierMinorTypeStrategic or Co-development Partner
Description

Biocluster partner supporting innovative projects in biotherapy and regenerative medicine in Western France.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Sister company within Clean Biologics group providing GMP virus-based process development and manufacturing services for biologics up to Phase III. Companies work together to offer integrated solutions from cell banking through to IMP/IND manufacturing.

Recent move8 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeBroad incumbent
Description

Global leader in bioanalytical testing services with deep pharmaceutical and biopharma testing offerings. Overlaps directly with Clean Cells' biosafety, viral safety, and cell bank testing services, but operates at vastly greater scale and across many other verticals.

TypeBroad incumbent
Description

Swiss-based global testing, inspection, and certification company with a life sciences division offering biosafety and cell banking services. Competes on the testing side of Clean Cells' portfolio while serving many other industries at much larger scale.

TypeBroad incumbent
Description

World's largest CDMO with integrated cell and gene therapy manufacturing and analytical services. Overlaps on cell/virus banking, biosafety testing, and GMP release for biologics and ATMPs, while offering much broader development and commercial manufacturing capabilities.

TypeBroad incumbent
Description

MilliporeSigma's biopharma testing services arm offering biosafety, viral clearance, and cell line characterization. Direct overlap with Clean Cells' testing portfolio, backed by Merck KGaA's global reach and broader bioprocessing consumables franchise.

TypeEmerging player
Description

US-based CDMO focused on plasmid DNA manufacturing and related services for gene therapy and DNA vaccines. Adjacent peer in the cell and gene therapy supply chain with comparable GMP expertise but narrower scope than Clean Cells.

TypeDirect peer
Description

French CDMO specializing in GMP manufacturing of viral vectors and cell therapies for gene and cell therapy developers. Adjacent peer that competes for ATMP customers' analytical and starting-material work, though it is more manufacturing-focused than testing-focused.

TypeDirect peer
Description

Sister company within the Clean Biologics group, providing GMP virus-based process development and manufacturing for biologics up to Phase III. Shares the same ownership and often co-sells integrated cell-banking-through-IMP solutions, making it the closest operational peer.

TypeBroad incumbent
Description

Global CDMO with strong cell and gene therapy capabilities, including viral vector manufacturing and analytical services. Competes for ATMP customers and offers bundled development-to-commercial solutions that can displace specialist QC providers.

TypeDirect peer
Description

French-headquartered specialist in virus and biosafety testing services for cell and gene therapy products. Directly competes with Clean Cells on viral safety testing, adventitious agent detection, and GMP lot release for ATMP developers.

TypeBroad incumbent
Description

Major global CRO/CDMO with dedicated Biologics Testing Solutions covering biosafety, lot release, and cell banking services. Competes for the same biopharma quality control wallet with broader discovery and manufacturing services.

Market position
Strengths4 records

Each record includes

Headline, Details, Source

Weaknesses4 records

Each record includes

Headline, Details, Source

Competitive moat5 records

Each record includes

Type, Details

Key risks5 records

Each record includes

Headline, Details, Source

Key highlights6 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers7 records

Each record includes

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

Segment8 records

Each record includes

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

Ideal customer profile5 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
No
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
Profiles4 records

Each record includes

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

Subsidiaries3 records

Each record includes

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

Compliance3 records

Each record includes

Name, Class, Description

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

Investors1 record

Each record includes

Name, Type, Date of entry, Rounds participated, Website

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

M&A3 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 →

Clean Cells

Biopharmaceutical Quality Control Servicesclean-cells.com

Clean Cells is a French CMO/CRO providing cGMP-compliant cell and virus bank manufacturing and biopharmaceutical quality control testing for vaccines, proteins, gene therapies, and cell therapies, serving 230+ global biopharma customers from its 5,300 m2 Montaigu-Vendée facility and US subsidiaries.

What Clean Cells does

Clean Cells is a France-headquartered biopharmaceutical CMO/CRO founded in 2000, specializing in cGMP-compliant manufacturing of cell and virus banks and quality control testing for biologics including vaccines, therapeutic proteins, gene therapies, and cell therapies. The company operates from a 5,300 m2 facility in Montaigu-Vendée (near Nantes) with 9 GMP production suites and BSL2/BSL3 laboratory capabilities, and supports clients in North America through subsidiaries KaryoLogic (acquired April 2025) and Stem Genomics (acquired June 2026). Its service portfolio covers the full product lifecycle from cell banking, virus seed stock production, and clonal selection through biosafety testing, product characterization, lot release testing, and secure long-term storage, with 250+ validated assays across potency, identity, purity, and biosafety dimensions.

The company serves 230+ biopharmaceutical customers worldwide, performing 7,000+ analyses annually, and holds a granted patent on a non-radioactive luminescent potency assay for cytolytic activity (extended to Europe and Canada). Clean Cells generates revenue through professional services contracts on a quote-based, B2B basis, with an enterprise field sales motion supported by participation in major industry conferences (BIO-Europe, ESACT, ESGCT, CPHI) and educational webinars. The business is part of the Clean Biologics group backed by healthcare-focused private equity firm ArchiMed (majority shareholder since October 2018), alongside sister company Naobios (viral vaccine CDMO acquired March 2019). Following the 2023 facility expansion and recent US-focused acquisitions, Clean Cells is positioned as one of the largest European providers of biopharmaceutical QC services and cell bank production, with 127-133 employees as of the most recent reporting.

Clean Cells firmographics

Firmographics
Name
Clean Cells
Legal name
Clean Cells
Website
http://www.clean-cells.com
Company type
Private
Founded year
2000
Operating status
Operating
Headcount range
101–250 employees
Short description
Clean Cells is a French CMO/CRO providing cGMP-compliant cell and virus bank manufacturing and biopharmaceutical quality control testing for vaccines, proteins, gene therapies, and cell therapies, serving 230+ global biopharma customers from its 5,300 m2 Montaigu-Vendée facility and US subsidiaries.
Ownership category
akta.pro rank

Clean Cells industry classification

Industry
Product category
Biopharmaceutical Quality Control Services
NAICS
Medical Laboratories (621511), Medical and Diagnostic Laboratories (6215), Medical and Diagnostic Laboratories (62151)
SIC
Services-Medical Laboratories (8071), Biological Products, (No Disgnostic Substances) (2836), Services-Testing Laboratories (8734)
akta.pro primary industry
Analytical Development & QC Testing (Release/Stability/Potency) (HLAGAGAF)
akta.pro secondary industries
Gene Therapy Analytical Testing & QC (potency, vg/ddPCR, infectivity, RCL/RCA) (HLAAACAK), Cell Therapy Quality, Analytics & Release Testing (potency, sterility, comparability) (HLAAABAK), Cell Therapy Manufacturing Services (GMP, autologous/allogeneic) (HLAAAKAC), GMP Manufacturing Support Services (QA/QMS, validation, documentation) (HLAAAKAH), Environmental Monitoring & Cleanroom Testing (GMP) (HLAGADAL)

Keywords

  • Biologics testing services
  • Cell bank manufacturing
  • Virus bank manufacturing
  • Biosafety testing services
  • Pharmaceutical quality control

Where Clean Cells is headquartered

Location

Headquarters

HQ city
Boufféré
HQ country
France
HQ region
Europe

Offices3 records

Markets served

Clean Cells business model

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

Revenue model

  1. Quality Control and Biosafety Testing Services: The company provides biological safety tests and quality control testing for biopharmaceutical products to assist in regulatory compliance. Services include biosafety testing, product characterization, raw material testing, cell bank testing, virus bank testing, and lot release testing.
  2. Cell and Virus Bank Manufacturing: Production of cell banks and GMP-grade BSL2/BSL3 virus seed stock for use as starting materials in biopharmaceutical manufacturing. Services include clonal selection, cell banking, and virus banking.
  3. Biologics Storage Services: Secure storage services for cell banks and virus banks with options for shared or dedicated containers, continuous temperature monitoring, and backup systems.
  4. Analytical Development: Development and validation of bespoke analysis tools for biopharmaceutical products, including custom assay development.

Go-to-market motion3 records

Distribution channels1 record

Marketing channels5 records

Clean Cells product offering

Product offering

Core offering

Clean Cells is a CMO/CRO providing GMP-compliant cell and virus bank manufacturing together with comprehensive quality control testing services for biopharmaceutical products. Its offering covers biosafety testing, product characterization, cell and virus bank testing, lot release testing, raw material testing, analytical development, and secure long-term storage, supporting vaccine, therapeutic protein, gene therapy, cell therapy, and ATMP developers from R&D through market release in compliance with worldwide regulatory agencies.

Product overview

Clean Cells operates as a comprehensive CMO/CRO providing integrated services for the biologics and biopharmaceutical industry. The core offering combines biologics biomanufacturing (cell banking, virus banking, clonal selection) with extensive biologics testing services (biosafety testing, product characterization, cell/virus bank testing, lot release testing, raw material testing). Additional services include analytical development, long-term storage solutions for cell and virus banks, phage therapy CDMO services, and viral safety testing for gene therapy products. The portfolio is complemented by the 2026 acquisition of Stem Genomics' iCS-digital PSC technology for stem cell genomic stability testing. Clean Cells serves global customers from facilities in France with US operations through subsidiaries KaryoLogic and Stem Genomics, offering a one-stop-shop solution from R&D through market release under GMP compliance.

Differentiator

Problem solved

Functional benefit

Products and services

  • Biologics Biomanufacturing Services Comprehensive manufacturing services for cell banks, virus banks, and clonal selection, including production of GMP or non-GMP Master and Working cell banks, virus seed stock manufacturing under BSL2/BSL3 conditions, and end of production cells generation for biopharmaceutical developers.
  • Biosafety Testing Comprehensive biosafety testing services including microbiology testing (sterility, mycoplasma, endotoxin), viral safety testing, and adventitious agent detection to ensure biological product safety and regulatory compliance for biopharmaceutical developers.
  • Product Characterization Full characterization services for biologics including impurity testing, potency testing (ADCC/CDC/cell-based assays including the patented cytolytic activity assay), and biologics identity testing, supporting regulatory compliance from R&D through market release.
  • Cell Bank Testing Comprehensive testing services for cell banks including sterility, mycoplasma, mycobacteria, adventitious agent detection (in-vivo, in-vitro), specific pathogen testing, retrovirus detection (electron microscopy, infectivity assays, qPERT), identity testing, and genetic stability assessment.
  • Virus Bank Testing Complete virus bank characterization services in GMP conditions ensuring safety, potency, and reliability, including comprehensive viral detection by qPCR covering more than 250 viruses.
  • Lot Release Testing Quality control testing services for lot release of biological products, ensuring product safety, identity, purity, and potency meet regulatory requirements before commercial distribution.
  • Raw Material Testing Testing services for raw materials used in biopharmaceutical manufacturing, ensuring quality and safety of starting materials and reagents.
  • Cell Bank Storage Long-term secure storage services for cell banks at ultra-low temperatures (below -145°C) using liquid or vapor-phase nitrogen tanks or ultra-low temperature freezers, with dedicated or shared container options and continuous temperature monitoring.
  • Virus Bank Storage Secure long-term storage for virus banks at temperatures as low as -80°C, including shared container storage with dedicated boxes or shelves, continuous temperature monitoring, externalized alarm systems, and backup freezer for added security.
  • Analytical Development Custom assay development and validation services for biopharmaceutical products in GMP and non-GMP settings, including implementation of innovative techniques such as digital PCR (dPCR) for quantification of nucleic acids.
  • Phage Therapy CDMO Services Contract development and manufacturing services for therapeutic bacteriophages, including process development, GMP manufacturing, and purification services for phage therapy products.
  • Viral Safety Testing for Gene Therapy Comprehensive GMP biosafety testing services for gene therapy products including recombinant lentiviral vectors (rLv), with detection of replication-competent lentiviral particles (RCL), and potency and safety characterization for ATMPs.
  • Stem Genomics iCS-digital PSC Genomic Stability Testing Next-generation genomic stability quality controls for human pluripotent stem cells (hPSCs) using the iCS-digital PSC technology platform, addressing genomic integrity requirements for advanced cell therapy developers.

Quantifiable outcome

  • 5,300 m2 facility quadruples analysis and production capacity
  • +3 more outcomes

Companies that use Clean Cells

Customer profile

Named customers7 records

Segments8 records

Ideal customer profiles5 records

Clean Cells technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature4 records

Clean Cells partnerships and signals

Strategic signal

Partnerships

Eight partnerships are on record, tiered core and minor.

  • Stem GenomicscoreStrategic or Co-development Partner · 18 June 2026Acquired in June 2026 to strengthen cell therapy quality control and expand US presence. Provider of next-generation quality controls for stem cell therapy including iCS-digital PSC technology platform. Works with 150+ clients worldwide including academic institutions, biotech companies, and core facilities. Operations in Montpellier, France and Durham, North Carolina.
  • KaryoLogic Inc.coreStrategic or Co-development Partner · 1 April 2025Acquired to accelerate expansion in US biologics market. US subsidiary of Clean Cells located in Durham, North Carolina, providing services to North American clients.
  • OSE Immunotherapeutics SAminorStrategic or Co-development PartnerCollaborative partner in HybridADCC project, a €2.4M funded initiative developing standardised ADCC assay for testing mouse monoclonal antibodies using hybrid human/mouse technology.
  • INSERM UMR1232/CNRSERL6001minorStrategic or Co-development PartnerResearch partner in HybridADCC collaborative project focused on developing standardised ADCC assay methodology for therapeutic antibody characterization.
  • MicroPiCell platformminorStrategic or Co-development PartnerAcademic platform partner in HybridADCC project providing expertise in cell technology for antibody development.
  • France BioleadminorOthersFounding member of France Biolead association supporting the production of biological medicines alongside major actors such as Sanofi, Servier, INSERM, CEA.
  • Atlanpole BiotherapiesminorStrategic or Co-development PartnerBiocluster partner supporting innovative projects in biotherapy and regenerative medicine in Western France.
  • NaobioscoreStrategic or Co-development PartnerSister company within Clean Biologics group providing GMP virus-based process development and manufacturing services for biologics up to Phase III. Companies work together to offer integrated solutions from cell banking through to IMP/IND manufacturing.

Scale indicators11 records

Recent moves8 records

Expansion highlights6 records

Clean Cells competitors and assessment

Company assessment

Broad incumbents

  • Eurofins Scientific: Global leader in bioanalytical testing services with deep pharmaceutical and biopharma testing offerings. Overlaps directly with Clean Cells' biosafety, viral safety, and cell bank testing services, but operates at vastly greater scale and across many other verticals.
  • SGS: Swiss-based global testing, inspection, and certification company with a life sciences division offering biosafety and cell banking services. Competes on the testing side of Clean Cells' portfolio while serving many other industries at much larger scale.
  • Lonza: World's largest CDMO with integrated cell and gene therapy manufacturing and analytical services. Overlaps on cell/virus banking, biosafety testing, and GMP release for biologics and ATMPs, while offering much broader development and commercial manufacturing capabilities.
  • BioReliance (MilliporeSigma): MilliporeSigma's biopharma testing services arm offering biosafety, viral clearance, and cell line characterization. Direct overlap with Clean Cells' testing portfolio, backed by Merck KGaA's global reach and broader bioprocessing consumables franchise.
  • Catalent: Global CDMO with strong cell and gene therapy capabilities, including viral vector manufacturing and analytical services. Competes for ATMP customers and offers bundled development-to-commercial solutions that can displace specialist QC providers.
  • Charles River Laboratories: Major global CRO/CDMO with dedicated Biologics Testing Solutions covering biosafety, lot release, and cell banking services. Competes for the same biopharma quality control wallet with broader discovery and manufacturing services.

Emerging players

  • VGXI: US-based CDMO focused on plasmid DNA manufacturing and related services for gene therapy and DNA vaccines. Adjacent peer in the cell and gene therapy supply chain with comparable GMP expertise but narrower scope than Clean Cells.

Direct peers

  • Yposkesi: French CDMO specializing in GMP manufacturing of viral vectors and cell therapies for gene and cell therapy developers. Adjacent peer that competes for ATMP customers' analytical and starting-material work, though it is more manufacturing-focused than testing-focused.
  • Naobios: Sister company within the Clean Biologics group, providing GMP virus-based process development and manufacturing for biologics up to Phase III. Shares the same ownership and often co-sells integrated cell-banking-through-IMP solutions, making it the closest operational peer.
  • Texcell: French-headquartered specialist in virus and biosafety testing services for cell and gene therapy products. Directly competes with Clean Cells on viral safety testing, adventitious agent detection, and GMP lot release for ATMP developers.

Market position

Strengths4 records

Weaknesses4 records

Competitive moat5 records

Key risks5 records

Key highlights6 records

Customer concentration

Clean Cells social profiles

Digital presence

Clean Cells compliance and trust

Trust signal

Compliance3 records

Clean Cells financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Clean Cells leadership team

Management profile

Number of profiles

Profiles4 records

Clean Cells subsidiaries and ownership

Company hierarchy

Subsidiaries3 records

Clean Cells funding detail

Funding detail

Funding overview

Funding rounds1 record

Investors1 record

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

Clean Cells M&A and investment

M&A and investment

M&A3 records

Investments

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

Frequently asked questions about Clean Cells

What does Clean Cells do?

Clean Cells is a CMO/CRO providing GMP-compliant cell and virus bank manufacturing together with comprehensive quality control testing services for biopharmaceutical products. Its offering covers biosafety testing, product characterization, cell and virus bank testing, lot release testing, raw material testing, analytical development, and secure long-term storage, supporting vaccine, therapeutic protein, gene therapy, cell therapy, and ATMP developers from R&D through market release in compliance with worldwide regulatory agencies.

Is Clean Cells a public or private company?

Clean Cells is a private company. It is classified as private equity controlled and is currently operating.

When was Clean Cells founded?

Clean Cells was founded in 2000. It employs 101 to 250 people.

Where is Clean Cells based?

Clean Cells is headquartered in Boufféré, France, in the Europe region.

How does Clean Cells make money?

Four revenue lines are on record. Quality Control and Biosafety Testing Services are the primary driver. The others are cell and Virus Bank Manufacturing, biologics Storage Services and analytical Development.

Who are Clean Cells's main competitors?

Broad incumbents on record are Eurofins Scientific, SGS, Lonza, BioReliance (MilliporeSigma), Catalent and Charles River Laboratories. VGXI is listed as an emerging player. Direct peers are Yposkesi, Naobios and Texcell.

Does Clean Cells have an API?

No public API is recorded for Clean Cells.

What industry is Clean Cells in?

Clean Cells's product category is Biopharmaceutical Quality Control Services. Its primary akta.pro industry code is HLAGAGAF, Analytical Development & QC Testing (Release/Stability/Potency), with a secondary code of HLAAACAK, Gene Therapy Analytical Testing & QC (potency, vg/ddPCR, infectivity, RCL/RCA). Its NAICS code is 621511 and its SIC code is 8071.

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GenengnewsClean Cells Broadens Viral Safety Testing Portfolio with NGSClean Cells launched NGS-based viral safety testing for viral vectors and recombinant preparations, and acquired French bioinformatics CRO Xegen. The acquisition consolidates bioinformatics capabilities to support NGS workflows, with Xegen's CEO joining as project manager. The company plans to extend the validated method to cell banks.Nelson Advisors BlogThis Week in European HealthTech, MedTech and Health AI: 14th August 2026The European HealthTech, MedTech, and Health AI sectors are experiencing significant developments, including the enforcement of the EU AI Act and the introduction of a fast-track pathway by the UK’s Medicines and Healthcare products Regulatory Agency (MHRA). Key funding rounds have been reported, focusing on deep-tech diagnostics and clinical infrastructure, with notable investments in companies like Qureight and Ahead Health. Additionally, consolidation trends are seen in the biopharma sector, particularly with Clean Cells acquiring Anaquant.The Mass Spectrometry Web PortalClean Cells SAS. (6/18/26). "Press Release: Clean Cells Acquires Stem Genomics to Strengthen Cell Therapy Quality Control and Expand US Presence". Montaigu-Vendée, near Nantes.Clean Cells acquired Stem Genomics, a stem cell therapy quality control provider, to expand its cell therapy testing platform. The deal adds genomic stability testing for human pluripotent stem cells and strengthens Clean Cells' US presence. The stem cell assay market is projected to grow from $4.6B in 2025 to $10.27B by 2035.The Mass Spectrometry Web PortalClean Cells SAS. (7/30/26). "Press Release: Clean Cells Acquires Anaquant to Expand Analytical Capabilities in Biomanufacturing Quality Control". Montaigu-Vendée, near Nantes.Clean Cells acquired Anaquant, a mass-spectrometry-based bioanalysis specialist, to expand its protein characterization capabilities. The deal adds Anaquant's ReadyBeads technology and client relationships, creating an end-to-end analytical offering from early-stage development to GMP testing. Financial terms were not disclosed.Tech.euEuropean tech weekly recap: €878M in weekly deals and key trends from H1 2026Last week, over 50 European tech funding deals worth more than €878 million were tracked, plus over 10 exits and M&A transactions. In H1 2026, European tech companies raised €44.1 billion across 1,740 deals, with the UK leading at €18.7 billion and AI startups securing €5.92 billion.Clean-CellsClean Cells acquires Anaquant to expand analytical capabilities in biomanufacturing quality controlClean Cells acquired Anaquant, a mass-spectrometry-based bioanalysis provider, to expand protein characterization capabilities. The deal includes Anaquant's ReadyBeads technology and client relationships, with financial terms undisclosed. The acquisition creates an end-to-end analytical offering from early-stage development to GMP testing.Tech.euClean Cells acquires Anaquant to expand biopharma quality control with mass spectrometry expertiseClean Cells acquired French biopharma quality control provider Anaquant, expanding its analytical platform with mass spectrometry expertise. The deal includes Anaquant's ReadyBeads technology for host cell protein profiling, enabling end-to-end analytical services from early-stage development to GMP testing.AnaquantClean Cells acquires Anaquant to expand analytical capabilities in biomanufacturing quality controlClean Cells acquired Anaquant, a mass-spectrometry-based bioanalysis specialist, to expand protein characterization capabilities. The deal includes Anaquant's ReadyBeads technology for HCP profiling, and financial terms were not disclosed. The acquisition creates an end-to-end analytical offering from early-stage development to GMP testing.PR NewswireWorldwide Virus Filtration Industry to 2026 - Featuring Asahi Kasei Medical, Clean Cells and Lonza Group Among OthersResearch and Markets has added a new market report titled "Global Virus Filtration Market 2020-2026" to its offerings, forecasting the global market to reach $6,275.3 million by 2026 with a 12.26% annual growth rate. The report profiles key industry players including Asahi Kasei Medical, Clean Cells, and Lonza Group, analyzing market dynamics driven by pharmaceutical R&D and the COVID-19 pandemic.