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Catalent

Full company profile

uuid0004zd5

Namestring
Catalent
Legal namestring
Catalent, Inc.
Websiteurl
catalent.com
Company typeenum
Private
Founded yearint
1933
Descriptiontext

Catalent is a global Contract Development and Manufacturing Organization (CDMO) serving pharmaceutical, biotechnology, and consumer health companies across the full drug lifecycle, from early-stage development through commercial manufacturing and clinical supply. The company's portfolio spans oral dose (including RP Scherer Softgel, OptiForm, spray drying, and micronization technologies), biologics (GPEX cell line development, SMARTag bioconjugation, OneBio integrated suite), cell therapy (autologous/allogeneic CAR-T, iPSC-derived therapies via the RheinCell platform, NK cells), gene therapy (UpTempo AAV and plasmid DNA manufacturing at commercial scale), specialty (inhalation, small molecule injectables), clinical supply services (OneHub portal, FastChain demand-led supply, FlexDirect direct-to-patient, CTSuccess planning), and self-care/consumer health (OTC, supplements, beauty). Catalent operates from more than 45 facilities across North America, Europe, Asia Pacific, and Latin America, with notable campuses at Harmans, Maryland (gene therapy), Princeton (cell therapy), Kansas City (biologics analytical and clinical supply), Morrisville/RTP (inhalation), Madison (mammalian cell line), and Gosselies, Belgium (cell therapy and plasmid DNA).

The business model is B2B professional services revenue earned through contract development, manufacturing, and supply agreements — quote-based pricing determined by project scope, complexity, scale, and contract length, with multi-year terms for commercial manufacturing and project-based engagement for clinical work. Catalent commercializes a set of proprietary technology platforms (GPEX, UpTempo, SMARTag, OptiForm, OneBio, iPSC, Qai) that differentiate its offering versus pure-play contract manufacturers. The company sells directly to enterprise customers through technical sales, scientific consultation, and strategic partnership agreements, supported by industry conference participation and thought leadership content. Approximately 2,400 of its ~15,000 employees are scientists and technicians.

Catalent was acquired by Novo Holdings A/S for $16.5 billion in December 2024, taking it private after years as a publicly traded NYSE-listed company under ticker CTLT. Ownership has shifted strategic emphasis toward fill-finish and prefilled syringe capacity for GLP-1 therapies, while the business has simultaneously undergone restructuring in cell and gene therapy — including layoffs at the Harmans, Maryland gene therapy plant and the announced closure of the Gosselies, Belgium cell therapy site — and has faced FDA regulatory scrutiny at the Catalent Indiana fill-finish facility that has delayed customer approvals. Leadership includes CEO Alessandro Maselli and CFO Matti Masanovich.

Short descriptiontext

Catalent is a global CDMO providing drug development, manufacturing, and clinical supply services across oral dose, biologics, cell therapy, gene therapy, injectables, and consumer health, serving pharma, biotech, and wellness companies from 45+ facilities worldwide. Privately held by Novo Holdings A/S since December 2024.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
5,001–10,000
akta.pro rankint
HeadquartersTampa, United States
HQ citystring
Tampa
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices14 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
contract development manufacturing, pharmaceutical CDMO services, biologics manufacturing, cell gene therapy, clinical supply services
Industry6 codes
1Drug Substance–Drug Product Integrated CDMO
CodeHLAGABAGPrimaryYes
2Biologics (mAbs/Recombinant Proteins) CDMO
CodeHLAGABACPrimaryNo
3Cell Therapy CDMO
CodeHLAGABADPrimaryNo
4Sterile Fill-Finish & Aseptic Manufacturing CDMO
CodeHLAGABAHPrimaryNo
5Clinical Trial Material (CTM) Manufacturing & Supply CDMO
CodeHLAGABAKPrimaryNo
6Packaging, Labeling & Serialization (Clinical/Commercial) CDMO
CodeHLAGABAJPrimaryNo
NAICS code3 codes
  • Pharmaceutical and Medicine Manufacturing3254
  • Biological Product (except Diagnostic) Manufacturing325414
  • Pharmaceutical Preparation Manufacturing325412
SIC code3 codes
  • Pharmaceutical Preparations2834
  • Biological Products, (No Disgnostic Substances)2836
  • Services-Commercial Physical & Biological Research8731
Product category
Pharmaceutical Contract Development and Manufacturing
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model1 record
1Contract Development and Manufacturing Services
TypeProfessional Services
Description

Catalent generates revenue through providing integrated CDMO services including drug substance manufacturing, drug product manufacturing, fill-finish services, clinical supply services, and commercial manufacturing. Services are provided on a project basis with long-term contracts for commercial manufacturing.

catalent.com
Marketing channels4 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, Infrastructure, Operations, Technology or R&D, Supply Chain
Pricing details1 tier
1Project-based CDMO services with custom pricing
ModelOtherBilling cadenceMulti-year contract
Notes

Pricing is determined through direct quotation based on specific project requirements, manufacturing scale, and service scope

catalent.com
GTM typeB2B
B2B
Offering typeServices
Services
Brand1 of 14 records shown
1OptiForm Total Supply
Description

Integrated development, manufacturing and clinical supply solution combining formulation, clinical manufacturing, forecasting, packaging, labeling, storage and distribution.

clinical.catalent.com
+13 more records
Core offering1 text field

Catalent is a global Contract Development and Manufacturing Organization (CDMO) that provides integrated pharmaceutical development, manufacturing, and clinical supply services across oral dose, biologics, cell therapy, gene therapy, specialty, and consumer health modalities. The company partners with pharma, biotech, and self-care innovators from early-stage development through commercial manufacturing, leveraging proprietary technology platforms such as GPEx, UpTempo, SMARTag, OptiForm, and iPSC. Services span drug substance and drug product manufacturing, fill-finish, clinical packaging and supply, regulatory support, and tech transfers across a network of 45+ facilities globally.

Differentiator
Functional benefit
Problem solved
Product overview1 text field

Catalent is a leading global Contract Development and Manufacturing Organization (CDMO) offering an integrated portfolio of pharma services organized around five core business units: Pharma Services (oral dose, biologics, specialty), Clinical Supply Services, and Self-Care/Consumer Health. The Pharma Services unit includes oral dosage development and manufacturing via OptiForm Solution Suite and Softgel Technologies; biologics development through OneBio Suite combining GPEx cell line development, drug substance manufacturing, and drug product fill-finish; and cell/gene therapy manufacturing leveraging iPSC, UpTempo plasmid DNA, and SMARTag bioconjugation platforms. Clinical Supply Services provides end-to-end clinical trial support including FastChain demand-led supply, FlexDirect direct-to-patient distribution, CTSuccess planning, and Case Management for advanced therapies, accessible through the OneHub digital portal. Specialty services cover inhalation and small molecule injectables. Qai represents the company's first enterprise AI deployment for quality management.

Product and service15 records
1Pharma Services
CategoryCore Business Unit
Description

Integrated CDMO solutions spanning oral dose, biologics, specialty and clinical supply. Services include tech transfers, commercial manufacturing, and regulatory support for pharmaceutical and biotech innovators.

2Oral Dose
CategoryService Offering
Description

Comprehensive oral dosage solutions including development, bioavailability enhancement, dose form design, manufacturing and analytical services for tablets, capsules, softgel, and orally disintegrating formats.

3Biologics
CategoryService Offering
Description

End-to-end biologics development and manufacturing including cell line development, process development, drug substance and drug product manufacturing, and analytical services.

4Cell Therapy
CategoryService Offering
Description

GMP manufacturing and development services for autologous and allogeneic cell therapies including CAR-T, NK cells, and iPSC-derived cell products, with commercial-scale manufacturing capabilities.

5Gene Therapy
CategoryService Offering
Description

Viral vector manufacturing and development services for AAV, lentiviral vectors, and gene therapies, including plasmid DNA manufacturing, process development, and GMP commercial manufacturing.

6Clinical Supply Services
CategoryService Offering
Description

Global clinical supply management including packaging, labeling, storage, distribution, cold chain services, and comparator sourcing for Phase I-IV clinical trials.

7Self-Care (Consumer Health)
CategoryService Offering
Description

Contract manufacturing for OTC products, dietary supplements, and beauty/personal care products including formulation, manufacturing, and packaging services.

8Specialty (Inhalation and Injectables)
CategoryService Offering
Description

Specialized delivery solutions including inhalation products (dry powder inhalers, nasal delivery) and small molecule injectables with advanced containment technologies.

9OptiForm Total Supply
CategoryIntegrated Solution
Description

Integrated development, manufacturing and clinical supply solution combining formulation, clinical manufacturing, forecasting, packaging, labeling, storage and distribution in a parallel approach.

10OneHub Portal
CategoryDigital Platform
Description

Customer portal providing visibility into clinical supply operations including production timelines, inventory alerts, shipment tracking, and document management with secure sharing capabilities.

11FastChain Demand Led Supply
CategoryService Solution
Description

Dynamic decentralized approach to secondary packaging, labeling and distribution of made-to-order patient kits based on actual site/patient demand with Pack to Stock, Pack to Order, and Hybrid models.

12FlexDirect Direct-to-Patient Services
CategoryService Solution
Description

Clinical supply services enabling direct shipment of investigational products to patients' homes, reducing need for in-person site visits through site-to-patient and pharmacy-direct models.

13Case Management Services
CategoryService Solution
Description

End-to-end supply chain coordination for cell and gene therapies including scheduling, shipment arrangement, chain of custody documentation, and 24/7 monitoring.

14CTSuccess Clinical Supply Planning
CategoryService Solution
Description

Clinical supply planning service using proprietary StartScore methodology to evaluate project complexity and provide tailored support for study execution.

15Qai
CategoryAI Product
Description

Enterprise AI-powered quality management tool integrating into existing quality workflows to accelerate root cause analysis, reduce repeat deviations, and improve reporting consistency across global manufacturing.

Scale indicator8 records

Each record includes

Type, Value, Description, Source

Partnership5 partners
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-06-18
Description

Expanded agreement for iPSC-derived CAR-NK cell therapies, strengthening Catalent's position in cell therapy manufacturing services.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-05-13
Description

Partnership for GMP clinical batch manufacturing of SIL204, next-generation siRNA therapy targeting mutated KRAS, at Catalent's facility in Limoges, France for Phase 2/3 trial in locally advanced pancreatic cancer.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-04-09
Description

Expanded partnership through amended commercial license agreement allowing Cartherics to use Catalent's cGMP-compliant iPSC line for manufacturing and commercializing CAR-NK cell therapies for cancer and endometriosis, including lead candidate CTH-401. Cartherics received FDA approval to use this cell line.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-03-31
Description

Global partnership for development and clinical manufacturing of iPSC-derived cell therapies targeting ocular and retinal diseases. Catalent provides GMP-compliant iPSC lines and manufacturing capabilities to support GelMEDIX's vision-restoring therapies through all clinical stages.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-02-18
Description

Strategic partnership to develop and manufacture TED-A9, a cell therapy for Parkinson's disease. Catalent utilizes its global capabilities in cell therapy development and GMP manufacturing to support S.Biomedics' pipeline from early development through clinical trials and market launch.

Recent move9 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Largest pure-play global CDMO offering biologics, cell & gene therapy, and small-molecule manufacturing across a comparable multi-modality footprint; competes head-to-head with Catalent in mammalian cell line, viral vector and oral dose services.

TypeBroad incumbent
Description

Operates one of the largest pharma services franchises globally via Patheon, covering drug substance, drug product, clinical supply and packaging; overlaps Catalent's integrated offering but sits within a much larger diversified life-sciences portfolio.

TypeDirect peer
Description

Korean large-mammalian biologics CDMO with massive single-site bioreactor capacity; competes directly with Catalent Biologics for mAb and recombinant protein programs from clinical through commercial supply.

TypeDirect peer
Description

Global biologics CDMO offering end-to-end services from cell line development to commercial manufacturing; competes with Catalent's OneBio Suite and GPEx cell line offering, particularly for Asia-Pacific and cost-sensitive programs.

TypeDirect peer
Description

Swiss CDMO specializing in oral solid dose APIs and drug products; competes directly with Catalent's Oral Dose business in small-molecule formulation and manufacturing.

TypeDirect peer
Description

European CDMO focused on oral solid dose, sterile fill-finish and biologics; competes with Catalent's European footprint across small-molecule and aseptic manufacturing services.

TypeDirect peer
Description

Global CDMO focused on clinical trial supply, commercial packaging and sterile fill-finish; directly overlaps Catalent's Clinical Supply Services and specialty/injectables offerings.

TypeBroad incumbent
Description

Diversified life-sciences services company with pharma manufacturing exposure through Q² Solutions and broader clinical/commercial services; partial overlap with Catalent's clinical supply and biologics analytics offerings.

TypeEmerging player
Description

Primarily a CRO/preclinical services firm but expanding into cell & gene therapy CDMO via its CDMO segment; competes with Catalent's CGT offerings in early-stage and clinical manufacturing.

TypeDirect peer
Description

Specialist CDMO for aseptic fill-finish of injectables and pre-filled syringes; directly competes with Catalent's sterile fill-finish and specialty injectable offerings, particularly for biologics and GLP-1 customers.

Market position
Strengths4 records

Each record includes

Headline, Details, Source

Weaknesses4 records

Each record includes

Headline, Details, Source

Competitive moat6 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 customers6 records

Each record includes

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

Segment3 records

Each record includes

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

Ideal customer profile3 records

Each record includes

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

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

AI capability2 records

Each record includes

Type, Description, Source

AI maturity
App detail

Has app

Feature9 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

Subsidiaries5 records

Each record includes

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

No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds1 record

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

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&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 →

Catalent

Pharmaceutical Contract Development and Manufacturingcatalent.com

Catalent is a global CDMO providing drug development, manufacturing, and clinical supply services across oral dose, biologics, cell therapy, gene therapy, injectables, and consumer health, serving pharma, biotech, and wellness companies from 45+ facilities worldwide. Privately held by Novo Holdings A/S since December 2024.

What Catalent does

Catalent is a global Contract Development and Manufacturing Organization (CDMO) serving pharmaceutical, biotechnology, and consumer health companies across the full drug lifecycle, from early-stage development through commercial manufacturing and clinical supply. The company's portfolio spans oral dose (including RP Scherer Softgel, OptiForm, spray drying, and micronization technologies), biologics (GPEX cell line development, SMARTag bioconjugation, OneBio integrated suite), cell therapy (autologous/allogeneic CAR-T, iPSC-derived therapies via the RheinCell platform, NK cells), gene therapy (UpTempo AAV and plasmid DNA manufacturing at commercial scale), specialty (inhalation, small molecule injectables), clinical supply services (OneHub portal, FastChain demand-led supply, FlexDirect direct-to-patient, CTSuccess planning), and self-care/consumer health (OTC, supplements, beauty). Catalent operates from more than 45 facilities across North America, Europe, Asia Pacific, and Latin America, with notable campuses at Harmans, Maryland (gene therapy), Princeton (cell therapy), Kansas City (biologics analytical and clinical supply), Morrisville/RTP (inhalation), Madison (mammalian cell line), and Gosselies, Belgium (cell therapy and plasmid DNA).

The business model is B2B professional services revenue earned through contract development, manufacturing, and supply agreements — quote-based pricing determined by project scope, complexity, scale, and contract length, with multi-year terms for commercial manufacturing and project-based engagement for clinical work. Catalent commercializes a set of proprietary technology platforms (GPEX, UpTempo, SMARTag, OptiForm, OneBio, iPSC, Qai) that differentiate its offering versus pure-play contract manufacturers. The company sells directly to enterprise customers through technical sales, scientific consultation, and strategic partnership agreements, supported by industry conference participation and thought leadership content. Approximately 2,400 of its ~15,000 employees are scientists and technicians.

Catalent was acquired by Novo Holdings A/S for $16.5 billion in December 2024, taking it private after years as a publicly traded NYSE-listed company under ticker CTLT. Ownership has shifted strategic emphasis toward fill-finish and prefilled syringe capacity for GLP-1 therapies, while the business has simultaneously undergone restructuring in cell and gene therapy — including layoffs at the Harmans, Maryland gene therapy plant and the announced closure of the Gosselies, Belgium cell therapy site — and has faced FDA regulatory scrutiny at the Catalent Indiana fill-finish facility that has delayed customer approvals. Leadership includes CEO Alessandro Maselli and CFO Matti Masanovich.

Catalent firmographics

Firmographics
Name
Catalent
Legal name
Catalent, Inc.
Website
https://catalent.com
Company type
Private
Founded year
1933
Operating status
Operating
Headcount range
5,001–10,000 employees
Short description
Catalent is a global CDMO providing drug development, manufacturing, and clinical supply services across oral dose, biologics, cell therapy, gene therapy, injectables, and consumer health, serving pharma, biotech, and wellness companies from 45+ facilities worldwide. Privately held by Novo Holdings A/S since December 2024.
Ownership category
akta.pro rank

Catalent industry classification

Industry
Product category
Pharmaceutical Contract Development and Manufacturing
NAICS
Pharmaceutical and Medicine Manufacturing (3254), Biological Product (except Diagnostic) Manufacturing (325414), Pharmaceutical Preparation Manufacturing (325412)
SIC
Pharmaceutical Preparations (2834), Biological Products, (No Disgnostic Substances) (2836), Services-Commercial Physical & Biological Research (8731)
akta.pro primary industry
Drug Substance–Drug Product Integrated CDMO (HLAGABAG)
akta.pro secondary industries
Biologics (mAbs/Recombinant Proteins) CDMO (HLAGABAC), Cell Therapy CDMO (HLAGABAD), Sterile Fill-Finish & Aseptic Manufacturing CDMO (HLAGABAH), Clinical Trial Material (CTM) Manufacturing & Supply CDMO (HLAGABAK), Packaging, Labeling & Serialization (Clinical/Commercial) CDMO (HLAGABAJ)

Keywords

  • Contract development manufacturing
  • Pharmaceutical CDMO services
  • Biologics manufacturing
  • Cell gene therapy
  • Clinical supply services

Where Catalent is headquartered

Location

Headquarters

HQ city
Tampa
HQ country
United States
HQ region
North America

Offices14 records

Markets served

Catalent business model

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

Revenue model

  1. Contract Development and Manufacturing Services: Catalent generates revenue through providing integrated CDMO services including drug substance manufacturing, drug product manufacturing, fill-finish services, clinical supply services, and commercial manufacturing. Services are provided on a project basis with long-term contracts for commercial manufacturing.

Pricing tiers

ModelBillingPrice
OtherMulti-year contractProject-based CDMO services with custom pricing

Go-to-market motion1 record

Distribution channels1 record

Marketing channels4 records

Catalent product offering

Product offering

Core offering

Catalent is a global Contract Development and Manufacturing Organization (CDMO) that provides integrated pharmaceutical development, manufacturing, and clinical supply services across oral dose, biologics, cell therapy, gene therapy, specialty, and consumer health modalities. The company partners with pharma, biotech, and self-care innovators from early-stage development through commercial manufacturing, leveraging proprietary technology platforms such as GPEx, UpTempo, SMARTag, OptiForm, and iPSC. Services span drug substance and drug product manufacturing, fill-finish, clinical packaging and supply, regulatory support, and tech transfers across a network of 45+ facilities globally.

Product overview

Catalent is a leading global Contract Development and Manufacturing Organization (CDMO) offering an integrated portfolio of pharma services organized around five core business units: Pharma Services (oral dose, biologics, specialty), Clinical Supply Services, and Self-Care/Consumer Health. The Pharma Services unit includes oral dosage development and manufacturing via OptiForm Solution Suite and Softgel Technologies; biologics development through OneBio Suite combining GPEx cell line development, drug substance manufacturing, and drug product fill-finish; and cell/gene therapy manufacturing leveraging iPSC, UpTempo plasmid DNA, and SMARTag bioconjugation platforms. Clinical Supply Services provides end-to-end clinical trial support including FastChain demand-led supply, FlexDirect direct-to-patient distribution, CTSuccess planning, and Case Management for advanced therapies, accessible through the OneHub digital portal. Specialty services cover inhalation and small molecule injectables. Qai represents the company's first enterprise AI deployment for quality management.

Differentiator

Problem solved

Functional benefit

Brands

  • OptiForm Total Supply: Integrated development, manufacturing and clinical supply solution combining formulation, clinical manufacturing, forecasting, packaging, labeling, storage and distribution.
  • OneHub Portal
  • FastChain Demand Led Supply
  • FlexDirect
  • CTSuccess
  • OptiForm Solution Suite
  • OneBio Suite
  • GPEx
  • SMARTag
  • UpTempo
  • Qai
  • OneXpress Solution
  • OptiDose Design Solution
  • Portfolio Accelerator

Products and services

  • Pharma Services Integrated CDMO solutions spanning oral dose, biologics, specialty and clinical supply. Services include tech transfers, commercial manufacturing, and regulatory support for pharmaceutical and biotech innovators.
  • Oral Dose Comprehensive oral dosage solutions including development, bioavailability enhancement, dose form design, manufacturing and analytical services for tablets, capsules, softgel, and orally disintegrating formats.
  • Biologics End-to-end biologics development and manufacturing including cell line development, process development, drug substance and drug product manufacturing, and analytical services.
  • Cell Therapy GMP manufacturing and development services for autologous and allogeneic cell therapies including CAR-T, NK cells, and iPSC-derived cell products, with commercial-scale manufacturing capabilities.
  • Gene Therapy Viral vector manufacturing and development services for AAV, lentiviral vectors, and gene therapies, including plasmid DNA manufacturing, process development, and GMP commercial manufacturing.
  • Clinical Supply Services Global clinical supply management including packaging, labeling, storage, distribution, cold chain services, and comparator sourcing for Phase I-IV clinical trials.
  • Self-Care (Consumer Health) Contract manufacturing for OTC products, dietary supplements, and beauty/personal care products including formulation, manufacturing, and packaging services.
  • Specialty (Inhalation and Injectables) Specialized delivery solutions including inhalation products (dry powder inhalers, nasal delivery) and small molecule injectables with advanced containment technologies.
  • OptiForm Total Supply Integrated development, manufacturing and clinical supply solution combining formulation, clinical manufacturing, forecasting, packaging, labeling, storage and distribution in a parallel approach.
  • OneHub Portal Customer portal providing visibility into clinical supply operations including production timelines, inventory alerts, shipment tracking, and document management with secure sharing capabilities.
  • FastChain Demand Led Supply Dynamic decentralized approach to secondary packaging, labeling and distribution of made-to-order patient kits based on actual site/patient demand with Pack to Stock, Pack to Order, and Hybrid models.
  • FlexDirect Direct-to-Patient Services Clinical supply services enabling direct shipment of investigational products to patients' homes, reducing need for in-person site visits through site-to-patient and pharmacy-direct models.
  • Case Management Services End-to-end supply chain coordination for cell and gene therapies including scheduling, shipment arrangement, chain of custody documentation, and 24/7 monitoring.
  • CTSuccess Clinical Supply Planning Clinical supply planning service using proprietary StartScore methodology to evaluate project complexity and provide tailored support for study execution.
  • Qai Enterprise AI-powered quality management tool integrating into existing quality workflows to accelerate root cause analysis, reduce repeat deviations, and improve reporting consistency across global manufacturing.

Companies that use Catalent

Customer profile

Named customers6 records

Segments3 records

Ideal customer profiles3 records

Catalent technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

AI capability2 records

Feature9 records

Catalent partnerships and signals

Strategic signal

Partnerships

Five partnerships are on record, tiered core.

  • CarthericscoreStrategic or Co-development Partner · 18 June 2026Expanded agreement for iPSC-derived CAR-NK cell therapies, strengthening Catalent's position in cell therapy manufacturing services.
  • Silexion TherapeuticscoreStrategic or Co-development Partner · 13 May 2026Partnership for GMP clinical batch manufacturing of SIL204, next-generation siRNA therapy targeting mutated KRAS, at Catalent's facility in Limoges, France for Phase 2/3 trial in locally advanced pancreatic cancer.
  • CarthericscoreStrategic or Co-development Partner · 9 April 2026Expanded partnership through amended commercial license agreement allowing Cartherics to use Catalent's cGMP-compliant iPSC line for manufacturing and commercializing CAR-NK cell therapies for cancer and endometriosis, including lead candidate CTH-401. Cartherics received FDA approval to use this cell line.
  • GelMEDIXcoreStrategic or Co-development Partner · 31 March 2026Global partnership for development and clinical manufacturing of iPSC-derived cell therapies targeting ocular and retinal diseases. Catalent provides GMP-compliant iPSC lines and manufacturing capabilities to support GelMEDIX's vision-restoring therapies through all clinical stages.
  • S.BiomedicscoreStrategic or Co-development Partner · 18 February 2026Strategic partnership to develop and manufacture TED-A9, a cell therapy for Parkinson's disease. Catalent utilizes its global capabilities in cell therapy development and GMP manufacturing to support S.Biomedics' pipeline from early development through clinical trials and market launch.

Scale indicators8 records

Recent moves9 records

Expansion highlights6 records

Catalent competitors and assessment

Company assessment

Direct peers

  • Lonza Group: Largest pure-play global CDMO offering biologics, cell & gene therapy, and small-molecule manufacturing across a comparable multi-modality footprint; competes head-to-head with Catalent in mammalian cell line, viral vector and oral dose services.
  • Samsung Biologics: Korean large-mammalian biologics CDMO with massive single-site bioreactor capacity; competes directly with Catalent Biologics for mAb and recombinant protein programs from clinical through commercial supply.
  • WuXi Biologics: Global biologics CDMO offering end-to-end services from cell line development to commercial manufacturing; competes with Catalent's OneBio Suite and GPEx cell line offering, particularly for Asia-Pacific and cost-sensitive programs.
  • Siegfried Holding: Swiss CDMO specializing in oral solid dose APIs and drug products; competes directly with Catalent's Oral Dose business in small-molecule formulation and manufacturing.
  • Recipharm: European CDMO focused on oral solid dose, sterile fill-finish and biologics; competes with Catalent's European footprint across small-molecule and aseptic manufacturing services.
  • PCI Pharma Services: Global CDMO focused on clinical trial supply, commercial packaging and sterile fill-finish; directly overlaps Catalent's Clinical Supply Services and specialty/injectables offerings.
  • Vetter Pharma: Specialist CDMO for aseptic fill-finish of injectables and pre-filled syringes; directly competes with Catalent's sterile fill-finish and specialty injectable offerings, particularly for biologics and GLP-1 customers.

Broad incumbents

  • Thermo Fisher Scientific (Patheon CDMO): Operates one of the largest pharma services franchises globally via Patheon, covering drug substance, drug product, clinical supply and packaging; overlaps Catalent's integrated offering but sits within a much larger diversified life-sciences portfolio.
  • IQVIA (Q² Solutions / Manufacturing Services): Diversified life-sciences services company with pharma manufacturing exposure through Q² Solutions and broader clinical/commercial services; partial overlap with Catalent's clinical supply and biologics analytics offerings.

Emerging players

  • Charles River Laboratories: Primarily a CRO/preclinical services firm but expanding into cell & gene therapy CDMO via its CDMO segment; competes with Catalent's CGT offerings in early-stage and clinical manufacturing.

Market position

Strengths4 records

Weaknesses4 records

Competitive moat6 records

Key risks5 records

Key highlights6 records

Customer concentration

Catalent social profiles

Digital presence

Catalent financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Catalent leadership team

Management profile

Number of profiles

Profiles4 records

Catalent subsidiaries and ownership

Company hierarchy

Subsidiaries5 records

Catalent funding detail

Funding detail

Funding overview

Funding rounds1 record

Investors1 record

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

Catalent 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 Catalent

What does Catalent do?

Catalent is a global Contract Development and Manufacturing Organization (CDMO) that provides integrated pharmaceutical development, manufacturing, and clinical supply services across oral dose, biologics, cell therapy, gene therapy, specialty, and consumer health modalities. The company partners with pharma, biotech, and self-care innovators from early-stage development through commercial manufacturing, leveraging proprietary technology platforms such as GPEx, UpTempo, SMARTag, OptiForm, and iPSC. Services span drug substance and drug product manufacturing, fill-finish, clinical packaging and supply, regulatory support, and tech transfers across a network of 45+ facilities globally.

Is Catalent a public or private company?

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

When was Catalent founded?

Catalent was founded in 1933. It employs 5,001 to 10,000 people.

Where is Catalent based?

Catalent is headquartered in Tampa, United States, in the North America region.

How does Catalent make money?

One revenue line is on record: contract Development and Manufacturing Services.

Who are Catalent's main competitors?

Direct peers on record are Lonza Group, Samsung Biologics, WuXi Biologics, Siegfried Holding, Recipharm, PCI Pharma Services and Vetter Pharma. Broad incumbents are Thermo Fisher Scientific (Patheon CDMO) and IQVIA (Q² Solutions / Manufacturing Services). Charles River Laboratories is listed as an emerging player.

Does Catalent have an API?

No public API is recorded for Catalent.

What industry is Catalent in?

Catalent's product category is Pharmaceutical Contract Development and Manufacturing. Its primary akta.pro industry code is HLAGABAG, Drug Substance–Drug Product Integrated CDMO, with a secondary code of HLAGABAC, Biologics (mAbs/Recombinant Proteins) CDMO. Its NAICS code is 3254 and its SIC code is 2834.

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Stock TitanTaysha, Catalent Sign TSHA-102 Rett Supply DealTaysha Gene Therapies and Catalent announced a supply agreement for TSHA-102, a gene therapy for Rett syndrome, with Catalent to serve as the primary commercial manufacturer following FDA approval. The agreement secures long-term manufacturing capacity at Catalent’s Maryland facility and builds on their partnership since 2020.BioSpaceTaysha Gene Therapies and Catalent Expand Strategic Partnership to Include Future Commercial Manufacturing Support of TSHA-102 Gene Therapy for Rett SyndromeTaysha Gene Therapies and Catalent announced a commercial supply agreement for TSHA-102, an investigational gene therapy for Rett syndrome, under which Catalent will serve as Taysha's primary commercial manufacturer following potential FDA approval. The agreement secures long-term manufacturing capacity and a scalable supply framework at Catalent's FDA-licensed facility in Maryland.GlobeNewswireTaysha Gene Therapies and Catalent Expand Strategic Partnership to Include Future Commercial Manufacturing Support of TSHA-102 Gene Therapy for Rett SyndromeTaysha Gene Therapies and Catalent announced a commercial supply agreement for TSHA-102, an investigational gene therapy for Rett syndrome, under which Catalent will serve as primary commercial manufacturer following potential FDA approval. The agreement secures long-term manufacturing capacity and a scalable supply framework, with BLA-enabling process performance qualification activities underway.SemaforBanks pay backhanded compliments to private credit | SemaforMajor banks including JPMorgan, Morgan Stanley, Deutsche Bank, Goldman Sachs, and Bank of Montreal are refinancing loans originally made by private credit firms, with Deutsche Bank selling $3 billion of fresh debt to refinance a Baker Tilly loan previously held by Blackstone and Blue Owl, while JPMorgan and Morgan Stanley are working on a $4 billion Catalent refinancing. The article argues this activity represents a backhanded validation of private credit underwriting, as banks would not compete for these borrowers at tighter spreads if they believed they were headed for trouble. The real risk for private lenders is adverse selection—losing their safest, most bankable borrowers to traditional banks while retaining weaker loans on their books.European BiotechnologySamsung Targets Swiss CDMO PolyPeptide in $1.8 Billion DealSamsung Biologics offered CHF44.31 per share in cash for Swiss peptide CDMO PolyPeptide, valuing it at about CHF1.46 billion. PolyPeptide's revenue rose 41.6% to €236.6 million in H1 2026, with full-year growth expected at 25-30%. The deal would expand Samsung's manufacturing into therapeutic peptides.OctusCatalent Lining Up $4.1B BSL Debt to Refi Massive Private Credit Debt Backing Novo Holdings Buyout; JPMorgan, Morgan Stanley Co-LeadingDrug manufacturer Catalent is arranging approximately $4.1 billion in broadly syndicated loan debt to refinance the private credit financing that backed Novo Holdings' $16.5 billion acquisition of the company in December 2024, with JPMorgan and Morgan Stanley co-leading the refinancing, according to sources. The refinancing will replace the private credit debt led by Ares and Blue Owl, which was one of the largest private credit transactions on record at the time of the deal. The transaction is expected to launch soon, though timing remains fluid and terms are subject to change.Longevity.TechnologyNanoscope, Catalent to manufacture and launch vision-restoring gene therapyCatalent and Nanoscope Therapeutics have expanded their collaboration to support late-phase clinical and commercial supply of MCO-010, an optogenetic gene therapy designed to restore vision in advanced retinal degenerative diseases including retinitis pigmentosa and Stargardt disease. Nanoscope reported positive RESTORE Phase 2b/3 results for retinitis pigmentosa and promising STARLIGHT Phase 2 outcomes for Stargardt disease, with a Phase 3 registrational trial planned for 2026 and a rolling FDA submission currently underway. The therapy has received multiple regulatory designations including FDA Fast Track, Orphan Drug, and RMAT, positioning it for potential accelerated approval and market entry.FiercePharmaCatalent sells UK facility to Codis, expands Nanoscope partnershipCodis has agreed to acquire Catalent's Nottingham facility in England for an undisclosed price, with the transaction expected to close by the end of Q3, positioning Codis to become a leading European provider of spray dry solutions. The site complements Codis' existing large-scale commercial spray-drying facility in Haverhill, U.K., and the company also operates manufacturing facilities in Missouri and Seymour, Indiana. Separately, Catalent expanded its partnership with Nanoscope Therapeutics to handle commercial packaging and distribution of their optogenetic gene therapy MCO-010, which is being developed to treat degenerative eye diseases such as retinitis pigmentosa and Stargardt disease.BioSpaceCatalent and Nanoscope Therapeutics Expand Partnership to Support Late-Phase Development and Commercial Supply of MCO-010Catalent and Nanoscope Therapeutics expanded their partnership to support late-phase clinical and commercial supply of MCO-010, with Catalent providing commercial-compliant packaging and distribution. A rolling FDA BLA submission is underway, and a Phase 3 registrational trial is planned for 2026.BioSpaceCatalent and Nanoscope Therapeutics Expand Partnership to Support Late-Phase Development and Commercial Supply of Lead Optogenetic Gene therapy, MCO-010Catalent and Nanoscope Therapeutics expanded their partnership to support late-phase development and commercial supply of MCO-010, an optogenetic gene therapy for retinal degenerative diseases. Catalent will provide commercial-compliant packaging and distribution, and has secured the commercial packaging validation program for Nanoscope's BLA, with a rolling FDA submission underway.