Towards Healthcare

Cell and Gene Therapy Thawing Equipment Key Players and Company Profile 2025

Date : 13 October 2025

Top Companies in the Cell and Gene Therapy Thawing Equipment Market

Cell and Gene Therapy Thawing Equipment Market Companies

  • Cytiva (Danaher)
  • BioLife Solutions
  • Barkey GmbH
  • Sartorius AG
  • Thermo Fisher Scientific
  • Helmer Scientific
  • Boekel Scientific
  • PHC Holdings Corporation
  • Eppendorf AG
  • Azenta Life Sciences (Brooks Life Sciences)
  • Cryoport Systems
  • BioCision LLC
  • Amerex Instruments
  • Glen Mills Inc.
  • Barkey GmbH & Co. KG
  • Custom Biogenic Systems
  • Boekel Scientific Inc.
  • Delta Development Team
  • Haier Biomedical
  • Stirling Ultracold

Company Profile

Company Headquarters Annual Revenue (Latest Year) Year
Thermo Fisher Scientific Waltham, Massachusetts, USA $42.88 billion 2024
Sartorius AG Göttingen, Germany €3.4 billion (≈$3.7 billion) 2024
Cytiva (Danaher Corporation) Marlborough, Massachusetts, USA (part of Danaher Life Sciences) ≈$3.3 billion 2024
PHC Holdings Corporation Tokyo, Japan ¥361.6 billion (≈$2.5 billion) 2024
Azenta Life Sciences (Brooks Life Sciences) Burlington, Massachusetts, USA $656 million 2024

Cytiva (Danaher)

Overview

  • Headquarters: Marlborough, Massachusetts, USA; major operations in Uppsala, Sweden.

  • Established as Cytiva in 2020 after Danaher acquired and rebranded GE Healthcare Life Sciences (roots trace back to Amersham).

  • Part of Danaher’s Life Sciences platform; portfolio spans bioprocessing hardware, consumables, and analytics (ÄKTA, Whatman, HyClone, Biacore).

Products

  • Bioprocessing systems & consumables (e.g., ÄKTA chromatography, single-use platforms).

  • Label-free interaction analysis with Biacore™ SPR instruments and software.

  • Filtration, cell culture media, and lab consumables (Amersham/Whatman).

Strengths

  • Deep installed base and trusted legacy brands (Amersham/Whatman/ÄKTA/Biacore).

  • Global footprint with R&D and manufacturing across ~40 countries.

  • Integration within Danaher unlocks operational excellence and M&A scale.

Opportunities

  • Growth in biologics and CGT manufacturing capacity requirements

  • Expansion of SPR and advanced analytics into discovery and QC workflows.

  • Partnerships with government/academia (e.g., Testa Center) to accelerate innovation.

Challenges

  • Exposure to bioprocessing inventory destocking cycles across pharma/biotech.

  • Competitive intensity from other full-line bioprocess suppliers.

  • Currency and regulatory complexities across large multi-region operations.

Recent developments

  • Continued innovation in Biacore™ SPR platforms and applications.

  • Ongoing portfolio and site investments under Danaher’s Life Sciences platform. 

  • Expanded customer support/content for label-free analysis workflows.

BioLife Solutions

Overview

  • Headquarters: Bothell, Washington, USA; founded 1987 (origins as Cryomedical Sciences; BioLife entity formed in 1998/2002). 

  • Developer of CGT bioproduction tools and services, focused on biopreservation media, freezers/thaw systems, and storage services.

  • Public company (Nasdaq: BLFS).

Products

  • CryoStor® & HypoThermosol® preservation media.

  • ThawSTAR® automated cell-thaw systems and ULT/cryogenic freezers portfolio.

  • SciSafe® biostorage and cold-chain monitoring/IT solutions.

Collaborations

  • CDMO Partnerships: Collaborates with contract development and manufacturing organizations to streamline supply chains

  • Therapy Sponsors: Works with therapy sponsors for integrated cell and gene therapy logistics

  • Research Collaborations: Engages with academic and industry partners for advanced biopreservation R&D

Strengths

  • Differentiated IP in preservation media with broad CGT adoption.

  • Complementary hardware + services model (freezers, storage, monitoring).

  • Recognized brand in CGT workflows and “best places to work” culture.

Opportunities

  • Scaling cell-processing revenue and recurring media usage as CGT approvals rise.

  • Portfolio optimization post-divestitures to focus on higher-margin lines.

  • Strategic partnerships with CDMOs and therapy sponsors for integrated supply.

Recent developments

  • FY2024 results: Cell Processing revenue $73.5M; 2025 total revenue guide $95.5–$99M (continuing ops).

  • Profitability improvements with 60% GAAP gross margin in Q4’24.

  • Portfolio emphasis on cell-processing tools and core media.

Barkey GmbH

Overview

  • Headquarters: Leopoldshöhe, Germany; founded 1980.

  • Specialist in medical warming and controlled-rate thawing devices used in transfusion, transplantation, and CGT. 

  • Devices deployed in 60+ countries across hospitals, blood banks, and research. 

Products

  • plasmatherm and related dry-heat thaw/warmer systems for plasma, blood, cells.

  • benchtop thawers for CGT workflows and cryobag handling. 

  • Accessories for safe, standardized warming procedures. 

Strategies

  • Product Diversification: Developing next-generation automated thawing systems compatible with a broader range of cryobags and materials.

  • Customer-Centric Service Model: Expanding technical service hubs in North America and Asia to improve global support and maintenance coverage.

  • Digital Integration: Introducing data-logging and connectivity features to monitor, record, and validate thawing processes for regulatory compliance and traceability.

Challenges

  • Competition from automated thaw systems by diversified life-science vendors. 

  • Need to validate across varied cell types and bag formats.

  • Scale-up of global service coverage as installed base grows.

Recent developments (M&A)

  • Acquired by Azenta, Inc. in 2022; deal broadened Azenta’s controlled-thaw capabilities. 

  • Post-deal, integration into Azenta’s CGT cold-chain platform. 

  • Continued international expansion of thaw products for CGT workflows. 

Sartorius AG

Overview

  • Headquarters: Göttingen, Germany; founded 1870. 

  • Global supplier of bioprocess solutions and lab products; DAX-listed. 

  • 2024 sales revenue approx. €3.4 billion; ~13.5k employees. 

Products

  • Single-use bioprocessing (bioreactors, filtration, fluid-management).

  • PAT/analytics and process development/testing services. 

  • Lab products & services (balances, pipettes, consumables). 

Mergers and Acquisitions

  • Sartorius has a strong M&A-driven growth strategy, consistently acquiring complementary businesses to expand its technology base and global footprint.

  • Recent acquisitions include Albumedix Ltd. (2022), strengthening Sartorius’s presence in recombinant albumin technology for cell culture and biopharma applications.

  • In 2023, Sartorius acquired a majority stake in Polyplus-transfection SA, enhancing its gene therapy and vaccine production capabilities with high-performance transfection reagents.

  • The company continues to pursue strategic partnerships and technology integrations, particularly in analytics and digital bioprocessing, to support next-generation biologics manufacturing.

Challenges

  • Exposure to cyclical capex and inventory digestion at biopharma customers.

  • Competitive pricing pressure in single-use and filtration. 

  • FX and input-cost volatility impacting margins.

Recent developments (facilities/partnerships)

  • Opened Center for Bioprocess Innovation near Boston (Marlborough, MA) in Nov 2024.

  • Continued portfolio expansion via targeted acquisitions/partnerships. 

  • Management commentary (2024 report): industry headwinds easing into 2025.

Thermo Fisher Scientific

Overview

  • Headquarters: Waltham, Massachusetts, USA; established in 2006 through the merger of Thermo Electron Corporation (founded 1956) and Fisher Scientific International (founded 1902).

  • Thermo Fisher Scientific is a global leader in scientific instrumentation, reagents, consumables, diagnostics, and CDMO (Contract Development and Manufacturing Organization) services, serving industries spanning healthcare, life sciences, environmental testing, and applied markets.

  • The company reported $42.88 billion in revenue in 2024, maintaining its position as one of the largest and most diversified life sciences companies worldwide.

Products

  • Analytical Instruments: Chromatography systems, mass spectrometers, electron microscopes, and molecular spectroscopy platforms used for advanced research and QC.

  • Life Sciences & Specialty Reagents: Consumables, reagents, and cell culture media for genomics, proteomics, and clinical diagnostics.

  • Pharma Services: End-to-end drug development, clinical research, and manufacturing solutions through PPD and Pharma Services Group.

Dominance

  • Thermo Fisher holds a commanding global market share in laboratory equipment, analytical instruments, and bioprocessing services, backed by an extensive customer base across biopharma, academia, and healthcare sectors.

  • The company’s scale and integration across the research-to-commercial value chain enable it to deliver unmatched continuity in scientific workflows—from discovery through manufacturing.

  • Its leadership in biomanufacturing, clinical research (via PPD), and specialty diagnostics positions Thermo Fisher as a dominant player in life sciences and pharmaceutical services globally.

Opportunities

  • Proteomics growth following Olink acquisition (2024). 

  • Capacity expansion and U.S. biomanufacturing investments.

  • AI-enabled workflows and automation across labs and CDMO units.

Challenges

  • Macroeconomic and FX headwinds on academic/biopharma spending. 

  • Regulatory/antitrust scrutiny on large acquisitions. 

  • Competition across multiple categories from major peers.

Recent developments (M&A/strategy)

  • Completed Olink acquisition (~$3.1B) in July 2024 to strengthen proteomics. 

  • Announced ~$2B U.S. investment program to expand manufacturing and R&D. 

  • FY2024 results released Jan 30, 2025 (revenue $42.88B). 

Helmer Scientific

Overview

  • Headquarters: Noblesville, Indiana, USA; founded 1977. 

  • Designs and manufactures medical-grade refrigerators, freezers, platelet storage, and blood bank equipment. 

  • Now part of Trane Technologies (acquired May 2023).

Products

  • Blood bank/clinical refrigerators, freezers, and platelet agitators/incubators. 

  • Plasma thawers and cell-processing support equipment. 

  • Service and aftermarket support for >125 countries. 

Strengths

  • Strong reputation in regulated, medical-grade cold storage. 

  • Large global installed base with service capability.

  • Backing from Trane accelerates scale, sustainability, and distribution. 

Opportunities

  • Cross-selling within Trane’s Life Science Solutions portfolio. 

  • Growth in precision temperature control for CGT and biobanking. 

  • Expanded service contracts and connected monitoring solutions. 

Challenges

  • Competition from diversified cold-chain OEMs. 

  • Compliance and validation requirements across geographies. 

  • Cost control on compressors/refrigerants amid environmental rules.

Boekel Scientific

Overview

  • Headquarters: Feasterville-Trevose (Philadelphia area), Pennsylvania, USA; founded 1868

  • Long-standing U.S. manufacturer of laboratory equipment and blood banking tools.

  • Private company with ISO-certified operations. 

Products

  • Incubators, water baths, ovens, shakers/rotators, and centrifuges. 

  • Blood banking and histology instruments and accessories. 

  • Custom/OEM lab equipment fabrication. 

Strengths

  • 150+ years of brand heritage and U.S. manufacturing. 

  • Broad portfolio for clinical and research labs. 

  • Ability to deliver bespoke/OEM builds. 

Opportunities

  • Refresh cycles in academic/clinical labs upgrading legacy equipment.

  • Export growth on durable, value-for-money devices.

  • Digital monitoring add-ons for regulated environments. 

Challenges

  • Competing vs. large diversified lab OEMs. 

  • Private-company scale limits vs. global rivals.

  • Margin pressure from input costs and supply constraints.

Recent developments (business updates)

  • Publicly available estimates place annual sales in the single-digit millions (private company; not formally disclosed).

  • Continued emphasis on U.S. manufacturing and product line extensions.

  • Ongoing OEM/custom equipment projects for niche workflows.

PHC Holdings Corporation

Overview

  • Headquarters: Tokyo, Japan; founded 2014 (Panasonic Healthcare legacy).

  • Global healthcare group with diagnostics, life-science equipment (e.g., PHCbi freezers), and healthcare IT. 

  • FY2024–FY2025 revenue ~¥354–¥362 billion. 

Products

  • PHCbi ultra-low temperature freezers and biomedical equipment. 

  • In-vitro diagnostics and clinical testing (group subsidiaries). 

  • Healthcare IT/diabetes care solutions. 

Strengths

  • Diversified healthcare portfolio across equipment, diagnostics, and IT. 

  • Large Asia-centric manufacturing base and distribution. 

  • Recognized PHCbi brand in ULT/biomedical cold storage. 

Opportunities

  • CGT and biobank demand for ULT/cryogenic storage. 

  • Digital health expansion in Japan and global markets. 

  • Portfolio optimization under integrated group strategy. 

Challenges

  • Currency fluctuations affecting imported components/export sales. 

  • Competition from global cold-storage and diagnostics leaders. 

  • Balancing growth with profitability across diverse business lines. 

Recent developments (strategy/reporting)

  • Published Integrated Report 2024 outlining mid- to long-term growth strategies.

  • Stable FY2025 revenue trend (~¥361.6B). 

  • Continued emphasis on global footprint and product breadth. 

Eppendorf AG (Eppendorf SE)

Overview

  • Headquarters: Hamburg, Germany; founded in 1945.

  • A private life-science company recognized globally for its pipettes, centrifuges, PCR systems, bioprocess equipment, and laboratory consumables.

  • Reported 2024 revenue of €980.3 million, reflecting its strong presence in laboratory instrumentation and consumables worldwide.

Products

  • Liquid-handling solutions including pipettes, tips, and dispensers for precise sample processing.

  • Sample-handling equipment such as centrifuges, tubes, and ultra-low temperature freezers.

  • PCR systems, bioshakers, and cell culture/bioprocess instruments supporting molecular biology and cell-based applications.

  • Digital lab solutions and services that connect instruments, streamline workflows, and enhance data integrity.

Strengths

  • Iconic global brand known for precision, reliability, and long product lifespans.

  • Broad market reach across academic, biopharmaceutical, and industrial laboratories.

  • Balanced portfolio combining high-margin consumables with durable laboratory equipment.

Opportunities

  • Implementation of the “Empowering Eppendorf” program launched in 2024 to drive operational efficiency and innovation.

  • Strong potential in digital lab automation and bioprocessing, aligned with the shift toward connected laboratory environments.

  • Expansion in emerging markets through channel investments and strategic local partnerships.

Challenges

  • Global slowdown in laboratory spending observed throughout 2024 impacting short-term growth.

  • Intense competition from diversified lab technology companies offering broader integrated portfolios.

  • Rising logistics and material costs creating margin pressures in international operations.

Recent Developments (Strategy)

  • Company-wide “Empowering Eppendorf” initiative introduced to boost efficiency, innovation, and sustainability.

  • 2024 marked as a challenging fiscal year, with proactive measures taken to position for growth recovery.

  • Ongoing portfolio expansion and customer service enhancements to strengthen global market presence.

Azenta Life Sciences (Brooks Life Sciences)

Overview

  • Headquarters: Burlington, Massachusetts, USA; founded in 1978 as Brooks Automation.

  • A leading provider of life sciences services and products, including genomics, biostorage, and automation solutions; rebranded as Azenta Life Sciences to reflect its life science focus.

  • Reported FY2024 revenue of approximately $656 million.

Products

  • Automated biostorage and cryogenic systems with advanced sample management and informatics.

  • Genomics and sequencing services (GENEWIZ) serving global research and biotech clients.

  • Controlled-thaw and CGT workflow devices added through the acquisition of Barkey GmbH.

Strengths

  • Blue-chip customer base across biotech, pharma, and research organizations.

  • A strong balance of services and product lines ensuring recurring revenue streams.

  • Proven acquisition track record with 29 successful integrations expanding capabilities and market reach.

Opportunities

  • Cross-selling Barkey’s thawing systems into its global biostorage customer base.

  • Growth in CGT logistics and end-to-end sample lifecycle management solutions.

  • Global expansion of genomics and sequencing service operations.

Challenges

  • Integration of multiple acquisitions while maintaining operational efficiency.

  • Rising competition in the genomics and biostorage service market.

  • High capital requirements for scaling cold-chain and automation infrastructure.

Recent Developments (M&A/Portfolio)

  • Completed acquisition of Barkey Holding GmbH to enhance CGT thawing and automation capabilities.

  • Reported FY2024 revenue of ~$656 million, reflecting continued growth from integrated product and service offerings.

  • Continued investment in site expansion and product development to strengthen its global footprint.

Cryoport Systems (Cryoport, Inc.)

Overview

  • Headquarters: Irvine, California, USA; founded in 1999.

  • Recognized as a global leader in temperature-controlled logistics and bioservices supporting the cell and gene therapy (CGT), reproductive medicine, and animal health sectors.

  • Reported 2024 revenue of $228.4 million, driven by strong performance in CGT logistics and storage.

Products

  • Cryogenic shippers, dewars, and monitoring technologies for validated transport of temperature-sensitive materials.

  • Bioservices and biostorage solutions, including GMP-compliant kitting and cold-chain management.

  • End-to-end supply chain design and program management tailored for advanced therapies.

Strengths

  • Industry-leading compliance and reliability in cold-chain logistics and chain-of-custody assurance.

  • Proven expertise supporting late-stage and commercial CGT programs globally.

  • Diversifying revenue base through the expansion of bioservices and integrated solutions.

Opportunities

  • Growth from new commercial CGT launches, boosting recurring shipments and service contracts.

  • Expansion of global storage and service nodes, improving customer accessibility and redundancy.

  • Strategic partnerships with therapy developers and CDMOs to provide end-to-end logistics infrastructure.

Challenges

  • Dependence on CGT clinical pipelines, leading to revenue fluctuations with program progress.

  • High capital expenditure to expand storage capacity and logistics hubs.

  • Growing competition from new entrants in specialty cold-chain logistics.

Recent Developments (Growth/Financials)

  • Reported FY2024 revenue of $228.4 million, marking continued year-over-year growth.

  • Trailing 12-month revenue of ~$238 million as of mid-2025.

  • Expanded Life Sciences Services division, strengthening its biostorage and bioservices capabilities.

BioCision LLC

Overview

  • A U.S.-based life sciences company focused on standardized, temperature-controlled handling of biomaterials, widely known for its CoolCell®, CoolBox®, and CryoPod® products.

  • The company has collaborated with Brooks (now Azenta) and partnered with distributors such as Corning for select product lines.

  • Operates as a portfolio brand with parts of its business acquired by Brooks; launched MedCision to advance automation solutions.

Products

  • CoolCell® alcohol-free, controlled-rate freezing containers for consistent cryopreservation.

  • CoolBox® ice-free benchtop cooling systems maintaining precise temperatures during sample handling.

  • CryoPod™ portable liquid nitrogen-based cryogenic carrier developed in collaboration with Brooks/Azenta.

Strengths

  • User-friendly and standardized thermal tools adopted across global laboratories.

  • Strong ecosystem connections with major automation and biostorage equipment providers.

  • Clear product benefits for reproducibility, sample integrity, and temperature consistency.

Opportunities

  • Integration into CGT standard operating procedures (SOPs) to minimize handling variability.

  • Collaborative development with logistics and storage providers for connected thermal workflows.

  • Training and educational initiatives promoting best practices in sample handling.

Challenges

  • Brand and ownership transitions following partial acquisition and integration into Brooks/Azenta.

  • Competition from lower-cost thermal tools produced by emerging labware manufacturers.

  • Limited public financial data due to private ownership structure.

Recent Developments (Collaboration/M&A)

  • Entered strategic collaboration with Brooks (Azenta) resulting in the launch of the CryoPod® carrier.

  • Brooks acquired BioCision’s key product lines, while BioCision established MedCision for automation technologies.

  • Continued distribution partnerships for its “Cool Lab” line to enhance global accessibility.

Market Growth

The global cell and gene therapy thawing equipment market size recorded US$ 0.96 billion in 2024, set to grow to US$ 1.1 billion in 2025 and projected to hit nearly US$ 3.56 billion by 2034, with a CAGR of 14.24% throughout the forecast timeline.

Funding and Investment

In May 2025, Stylus Medicine, a biotech startup, raised US$85 million in funding to launch a new class of in vivo genetic medicines that address the challenges associated with the production and delivery of ex vivo gene editing therapies. The first US$40 million Series A round of funding for the company was led by Khosla Ventures and RA Capital. Together with Johnson & Johnson Innovation-IJDC, Chugai Venture Fund, and Eli Lilly, these parties also backed a US$45 million extension.

Government Initiatives and Adoption of Inorganic Strategies

In July 2025, the Centers for Medicare & Medicaid Services (CMS) announced that 33 states, along with the District of Columbia and Puerto Rico, will join the Cell and Gene Therapy (CGT) Access Model, a daring new strategy for providing state-of-the-art treatments to Medicaid-eligible individuals with sickle cell disease. Access to transformative care has been greatly increased in participating states, which account for about 84% of Medicaid beneficiaries with the condition. This agreement is a significant victory for Medicaid to give patients new access to innovative treatments for sickle cell disease and for American patients, as stated by the U.S. Health and Human Services Secretary Robert F. Kennedy, Jr.

Value Chain Analysis of Cell and Gene Therapy Thawing Equipment Market

R&D

  • Market & clinical needs analysis - map therapy types, volumes, and clinical workflows.
  • Specification & regulatory mapping - define performance metrics (temperature ramp, uniformity), compliance (GMP, ISO 13485), data/traceability needs.
  • Concept design & risk assessment - thermal modelling, materials selection, risk (FMEA).
  • Prototype development - hardware + embedded/software for monitoring and audit trails.
  • In-lab biological testing - cell viability, potency surrogates, contamination/challenge testing.
  • Usability/human factors testing - simulated clinical workflows & operator training needs.
  • Verification & validation - bench verification, IQ/OQ/PQ, reliability testing.
  • Design freeze & regulatory dossier prep - technical file for notified bodies / 510(k)/de novo pathways or device modules supporting combination products

Typical organizations active in R&D (examples): university translational centres and hospitals (e.g., academic medical centres doing cell therapy research), equipment OEM R&D groups and engineering consultancies, biotech companies developing therapies (internal device/assay needs), and specialized test labs/CROs. Large industry names that commonly participate across device/therapy tool development include Thermo Fisher Scientific, Cytiva, Sartorius, BioLife Solutions, BioCision, plus many smaller specialized device startups.

Clinical Trials & Approval

  • Preclinical data collection - safety/compatibility data for device + thawed product.
  • Regulatory engagement - pre-submission meetings to define required evidence (FDA/EMA/PMDA).
  • Clinical site selection & training - equip and train sites on thawing workflows for trial use.
  • Trial conduct - device used per protocol; data collection on performance and any device-related adverse events.
  • Regulatory submission & review - include device validation and human factors data in filing.
  • Post-approval surveillance - vigilance, complaint handling, periodic safety updates.

Typical organizations involved: regulatory agencies (FDA, EMA, PMDA, Health Canada), clinical CROs and specialized cell/gene therapy CROs (ICON, Parexel, PPD, specialized academic trial networks), major clinical centres and hospitals running trials (e.g., major cancer centres), and regulatory/QA consultancies that prepare submissions.

Patient service & support

  • Therapy logistics & scheduling - coordinate thaw timing with infusion and patient arrival.
  • Specialty pharmacy & preparation - pharmacy handles thawing instructions/controls or hands the device to the clinic staff.
  • Point-of-care thawing & administration - trained nurses/technicians perform thawing and infusion; device logs preserved.
  • Patient follow-up & support programs - education, adverse-event monitoring, reimbursement/coverage assistance.
  • Maintenance & field service - preventive maintenance, calibration, rapid service response to avoid therapy delays.

Typical organizations/examples: specialty logistics and cold-chain providers (Cryoport, Marken, World Courier), specialty pharmacies and distributors (AmerisourceBergen, Cardinal Health, McKesson in distribution/support roles), pharma company patient support programs (therapy sponsors such as Novartis, Gilead/Kite, Bristol Myers Squibb run PSPs for approved cell therapies), and hospital infusion centres/clinical teams.

Latest Announcement by Industry Leaders

In July 2025, Adrian Stecyk, Chief Executive Officer of Myrtelle, stated that Myrtelle Inc., a trailblazing clinical-stage gene therapy business committed to transforming neurodegenerative disease treatment, declared the official start of commercial-stage production of its first-of-its-kind oligotrophic recombinant adeno-associated virus (rAAV) gene therapy product, created especially for Canavan disease (CD). This significant accomplishment brings Myrtelle treatment one step closer to the market and patients in dire need of it.

Recent Development in the Cell and Gene Therapy Thawing Equipment Market

In April 2025, the current capabilities of AGC Biologics will be enhanced by the new Cell and Gene Technologies Division, which will also assist developers who require capacity, scientific capabilities, and technically skilled cell and gene CDMO operators. With a vast global development and manufacturing network spread across three regions (Milan, Italy; Longmont, CO, USA; Yokohama, Japan), the new AGC Biologics Cell and Gene Technologies Division offers unmatched support and scientific capability, while other cell and gene CDMOs are closing locations and reducing their workforce.

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