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Cambrex

Full company profile

uuid0007v2q

Namestring
Cambrex
Legal namestring
Cambrex Corporation
Websiteurl
cambrex.com
Company typeenum
Private
Founded yearint
1980
Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
1,001–5,000
akta.pro rankint
HeadquartersEast Rutherford, United States
HQ citystring
East Rutherford
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices10 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
contract development manufacturing, active pharmaceutical ingredients, drug substance services, drug product formulation, analytical testing services
Industry4 codes
1Small-Molecule API & Intermediates CDMO
CodeHLAGABAAPrimaryYes
2Small-Molecule Drug Product (Solid/Oral/Parenteral) CDMO
CodeHLAGABABPrimaryNo
3Clinical Trial Material (CTM) Manufacturing & Supply CDMO
CodeHLAGABAKPrimaryNo
4Drug Substance–Drug Product Integrated CDMO
CodeHLAGABAGPrimaryNo
NAICS code1 code
  • Medicinal and Botanical Manufacturing325411
SIC code3 codes
  • Pharmaceutical Preparations2834
  • Medicinal Chemicals & Botanical Products2833
  • Services-Testing Laboratories8734
Product category
Pharmaceutical Contract Development and Manufacturing (CDMO)
Social media profiles2 records
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model5 records
1Drug Substance Development and Manufacturing
TypeProfessional Services
Description

Custom API development and manufacturing services including process development, scale-up, and commercial manufacturing. Revenue generated through project-based contracts, development fees, manufacturing fees, and potentially milestone payments tied to clinical and regulatory milestones.

cambrex.com
2Generic API Manufacturing
TypeOne Time License
Description

Supply of generic active pharmaceutical ingredients from catalog products and custom manufacturing. Revenue from product sales of generic APIs, intermediates, derivatives, and chiral compounds.

cambrex.com
3Analytical Services
TypeProfessional Services
Description

Comprehensive analytical testing and characterization services including method development, validation, stability testing, and microbiology services.

cambrex.com
4Drug Product Services
TypeProfessional Services
Description

Formulation development and clinical trial manufacturing services from early-phase through commercial scale, including tablet and capsule manufacturing.

cambrex.com
5Stability Storage Services (via Q1 Scientific)
TypeManaged Services
Description

Pharmaceutical stability storage and sample management services through Q1 Scientific subsidiary.

cambrex.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, Operations, Infrastructure, Technology or R&D, Supply Chain, Marketing or Sales
Pricing details1 tier
1Custom project-based pricing
ModelOtherBilling cadenceMulti-year contract
Notes

Pricing is negotiated on a project-by-project basis based on scope of services, development phase, manufacturing scale, and specific client requirements.

cambrex.com
GTM typeB2B
B2B
Offering typeServices
Services
Brand1 of 2 records shown
1Snapdragon Chemistry
Description

Specialized process development, flow chemistry, GMP manufacturing, custom peptide synthesis, complex synthetics, continuous process technologies, and reactor build and design services.

cambrex.com
+1 more record
Core offering1 text field

Cambrex is a global contract development and manufacturing organization (CDMO) that develops and manufactures active pharmaceutical ingredients (APIs) and drug products for pharmaceutical and biotech clients. The company provides end-to-end drug substance services (custom and generic API development and manufacturing, peptides, HPAPIs, controlled substances, biocatalysis, continuous flow), drug product services (oral solid dose formulation and clinical trial manufacturing), and analytical services (method development, stability testing, microbiology) across facilities in North America and Europe.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 5 values shown
  • Process mass intensity reduced by approximately 80% in organocatalytic process for obicetrapib
+4 more records
Product overview1 text field

Cambrex is a global contract development and manufacturing organization (CDMO) offering integrated drug substance and drug product services across the entire drug lifecycle. The portfolio is organized around three core pillars: Drug Substance Services (custom API development and manufacturing, generic APIs, specialty solutions including continuous flow, biocatalysis, HPAPIs, controlled substances, and complex synthetics), Analytical Services (comprehensive testing, solid state chemistry, stability storage via Q1 Scientific subsidiary, and microbiology), and Drug Product Services (formulation development and clinical trial manufacturing). The company has expanded capabilities through acquisitions including Snapdragon Chemistry (flow chemistry, custom peptides, complex synthetics, proprietary Z-Flow™ LPPS technology and LabOS platform for automated process development) and Q1 Scientific (stability storage). Services span from early-phase IND enabling through commercial manufacturing, covering over 90 generic APIs, controlled substances, and specialized peptide/oligonucleotide manufacturing.

Product and service7 records
1Drug Substance Services
CategoryDrug Substance Development and Manufacturing
Description

Comprehensive drug substance development and manufacturing services including custom API development, custom API manufacturing, generic API manufacturing, and specialty solutions (biocatalysis, continuous flow, highly potent APIs, controlled substances, complex synthetics, crystallization) for pharmaceutical and biotech clients.

2Analytical Services
CategoryAnalytical Testing Services
Description

Full suite of analytical testing services including method development and validation, release and ICH stability testing, material characterization, elemental impurities, compendial testing, impurity identification, nitrosamine testing, extractables and leachables testing, and reference standards.

3Drug Product Services
CategoryDrug Product Development and Manufacturing
Description

Drug product development and manufacturing including formulation development and clinical trial manufacturing for oral solid dose formulations (tablets, capsules) at early through late phases for pharmaceutical clients.

4Generic API Manufacturing
CategoryGeneric API Manufacturing
Description

Leading global supplier of generic APIs from sites in Italy, Sweden, and the USA. Portfolio of over 90 generic APIs, intermediates, derivatives, and chiral compounds including controlled substances, serving generic pharmaceutical firms requiring off-patent API supply.

5Peptide Development and Manufacturing
CategoryPeptide Manufacturing
Description

Cutting-edge peptide development and manufacturing combining solid phase synthesis (SPPS) and liquid phase peptide synthesis (LPPS) capabilities for early-stage clinical development through large-scale GMP manufacturing, meeting growing demand for peptide-based therapeutics.

6Snapdragon Chemistry Services
CategorySpecialty Chemistry Services
Description

Specialized chemistry solutions provider offering process development, GMP manufacturing, flow chemistry, custom peptide synthesis, complex synthetics, and reactor build and design services using advanced software and equipment for biopharmaceutical clients.

7Q1 Scientific Stability Storage
CategoryStability Storage Services
Description

Stability storage and sample management company providing pharmaceutical storage conditions meeting ICH Q1A requirements through walk-in and reach-in chambers for pharmaceutical and medical device companies.

Scale indicator9 records

Each record includes

Type, Value, Description, Source

Partnership6 partners
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-07-07
Description

Collaboration on development of sustainable organocatalytic process for obicetrapib, resulting in American Chemical Society Green Chemistry Challenge Award. Achieved 80% PMI reduction, 70% cycle time reduction, and 50% cost reduction in manufacturing.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Technology transfer and process development collaboration for danicopan, a complement Factor D inhibitor for paroxysmal nocturnal hemoglobinuria. Included significant process improvements in yield, PMI, and cycle times.

Strategic tierCoreTypeOEM/ Whitelabel/ Licensing Partner
Description

Cambrex company providing stability storage and sample management capabilities. Q1 Scientific offers pharmaceutical storage conditions meeting ICH Q1A requirements through walk-in and reach-in chambers.

Strategic tierMinorTypeOthers
Description

Corporate Power Purchase Agreement (CPPA) partnership through Q1 Scientific to source renewable electricity from Cronalaght Wind Farm, covering approximately 50% of Waterford site electricity demand.

Strategic tierCoreTypeOEM/ Whitelabel/ Licensing Partner
Description

Acquired by Cambrex, Snapdragon operates as a Cambrex company specializing in process development, continuous flow chemistry, and advanced manufacturing technologies including Z-Flow LPPS.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Co-authored study on RIPK1 inhibitor oditrasertib demonstrating continuous flow manufacturing process for pharmaceutical production.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Global CDMO offering drug substance and drug product services across small molecules, peptides, and biologics. Most directly comparable to Cambrex as a leading one-stop-shop CDMO serving pharma and biotech customers.

TypeDirect peer
Description

Major CDMO with drug substance, drug product, and clinical supply capabilities. Comparable to Cambrex in providing integrated development and manufacturing services to large pharma and biotech clients.

TypeBroad incumbent
Description

Through Patheon and its pharma services division, Thermo Fisher offers comprehensive CDMO services including API, drug product, and clinical supply. A scaled, diverse incumbent competing with Cambrex across drug substance and drug product.

TypeDirect peer
Description

Swiss-based CDMO specializing in small-molecule API manufacturing and drug product services. Highly comparable to Cambrex's custom API, generic API, and oral solid dose drug product offerings.

TypeDirect peer
Description

European CDMO with API and drug product manufacturing capabilities. Comparable to Cambrex as a mid-sized CDMO serving both innovator and generic pharma customers.

TypeDirect peer
Description

Global CRO/CDMO with extensive small-molecule and biologics capabilities. A peer across the drug development and manufacturing value chain, particularly for biotech customers.

TypeBroad incumbent
Description

Provides discovery, preclinical, and manufacturing services to pharma and biotech. Overlaps with Cambrex in analytical and drug substance support and competes for biotech development budgets.

TypeOthers
Description

Global laboratory testing services provider with strong pharma/biopharma analytical and CMC testing capabilities. Comparable to Cambrex's analytical services and Q1 Scientific stability storage offerings.

TypeEmerging player
Description

South Korea-based large-scale CDMO expanding from biologics into synthetic and oligonucleotide manufacturing. An emerging adjacency to Cambrex in the contract API manufacturing space.

TypeDirect peer
Description

Specialist CDMO in peptide and oligonucleotide API manufacturing. Most directly comparable to Cambrex's peptide platform (Z-Flow LPPS) and incremental peptide capacity at Karlskoga.

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 highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers4 records

Each record includes

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

Segment4 records

Each record includes

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

Ideal customer profile3 records

Each record includes

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

Technology focused
No
API detail
Has APIbool
No

Docs URL, Description

AI capability6 records

Each record includes

Type, Description, Source

AI maturity
App detail

Has app

Feature7 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles8 records

Each record includes

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

Subsidiaries2 records

Each record includes

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

Compliance15 records

Each record includes

Name, Class, Description

Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds

Each record includes

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

Investors

Each record includes

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

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

M&A6 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 →

Cambrex

Pharmaceutical Contract Development and Manufacturing (CDMO)cambrex.com

Cambrex firmographics

Firmographics
Name
Cambrex
Legal name
Cambrex Corporation
Website
https://cambrex.com
Company type
Private
Founded year
1980
Operating status
Operating
Headcount range
1,001–5,000 employees
Ownership category
akta.pro rank

Cambrex industry classification

Industry
Product category
Pharmaceutical Contract Development and Manufacturing (CDMO)
NAICS
Medicinal and Botanical Manufacturing (325411)
SIC
Pharmaceutical Preparations (2834), Medicinal Chemicals & Botanical Products (2833), Services-Testing Laboratories (8734)
akta.pro primary industry
Small-Molecule API & Intermediates CDMO (HLAGABAA)
akta.pro secondary industries
Small-Molecule Drug Product (Solid/Oral/Parenteral) CDMO (HLAGABAB), Clinical Trial Material (CTM) Manufacturing & Supply CDMO (HLAGABAK), Drug Substance–Drug Product Integrated CDMO (HLAGABAG)

Keywords

  • Contract development manufacturing
  • Active pharmaceutical ingredients
  • Drug substance services
  • Drug product formulation
  • Analytical testing services

Where Cambrex is headquartered

Location

Headquarters

HQ city
East Rutherford
HQ country
United States
HQ region
North America

Offices10 records

Markets served

Cambrex business model

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

Revenue model

  1. Drug Substance Development and Manufacturing: Custom API development and manufacturing services including process development, scale-up, and commercial manufacturing. Revenue generated through project-based contracts, development fees, manufacturing fees, and potentially milestone payments tied to clinical and regulatory milestones.
  2. Generic API Manufacturing: Supply of generic active pharmaceutical ingredients from catalog products and custom manufacturing. Revenue from product sales of generic APIs, intermediates, derivatives, and chiral compounds.
  3. Analytical Services: Comprehensive analytical testing and characterization services including method development, validation, stability testing, and microbiology services.
  4. Drug Product Services: Formulation development and clinical trial manufacturing services from early-phase through commercial scale, including tablet and capsule manufacturing.
  5. Stability Storage Services (via Q1 Scientific): Pharmaceutical stability storage and sample management services through Q1 Scientific subsidiary.

Pricing tiers

ModelBillingPrice
OtherMulti-year contractCustom project-based pricing

Go-to-market motion1 record

Distribution channels1 record

Marketing channels5 records

Cambrex product offering

Product offering

Core offering

Cambrex is a global contract development and manufacturing organization (CDMO) that develops and manufactures active pharmaceutical ingredients (APIs) and drug products for pharmaceutical and biotech clients. The company provides end-to-end drug substance services (custom and generic API development and manufacturing, peptides, HPAPIs, controlled substances, biocatalysis, continuous flow), drug product services (oral solid dose formulation and clinical trial manufacturing), and analytical services (method development, stability testing, microbiology) across facilities in North America and Europe.

Product overview

Cambrex is a global contract development and manufacturing organization (CDMO) offering integrated drug substance and drug product services across the entire drug lifecycle. The portfolio is organized around three core pillars: Drug Substance Services (custom API development and manufacturing, generic APIs, specialty solutions including continuous flow, biocatalysis, HPAPIs, controlled substances, and complex synthetics), Analytical Services (comprehensive testing, solid state chemistry, stability storage via Q1 Scientific subsidiary, and microbiology), and Drug Product Services (formulation development and clinical trial manufacturing). The company has expanded capabilities through acquisitions including Snapdragon Chemistry (flow chemistry, custom peptides, complex synthetics, proprietary Z-Flow™ LPPS technology and LabOS platform for automated process development) and Q1 Scientific (stability storage). Services span from early-phase IND enabling through commercial manufacturing, covering over 90 generic APIs, controlled substances, and specialized peptide/oligonucleotide manufacturing.

Differentiator

Problem solved

Functional benefit

Brands

  • Snapdragon Chemistry: Specialized process development, flow chemistry, GMP manufacturing, custom peptide synthesis, complex synthetics, continuous process technologies, and reactor build and design services.
  • Q1 Scientific

Products and services

  • Drug Substance Services Comprehensive drug substance development and manufacturing services including custom API development, custom API manufacturing, generic API manufacturing, and specialty solutions (biocatalysis, continuous flow, highly potent APIs, controlled substances, complex synthetics, crystallization) for pharmaceutical and biotech clients.
  • Analytical Services Full suite of analytical testing services including method development and validation, release and ICH stability testing, material characterization, elemental impurities, compendial testing, impurity identification, nitrosamine testing, extractables and leachables testing, and reference standards.
  • Drug Product Services Drug product development and manufacturing including formulation development and clinical trial manufacturing for oral solid dose formulations (tablets, capsules) at early through late phases for pharmaceutical clients.
  • Generic API Manufacturing Leading global supplier of generic APIs from sites in Italy, Sweden, and the USA. Portfolio of over 90 generic APIs, intermediates, derivatives, and chiral compounds including controlled substances, serving generic pharmaceutical firms requiring off-patent API supply.
  • Peptide Development and Manufacturing Cutting-edge peptide development and manufacturing combining solid phase synthesis (SPPS) and liquid phase peptide synthesis (LPPS) capabilities for early-stage clinical development through large-scale GMP manufacturing, meeting growing demand for peptide-based therapeutics.
  • Snapdragon Chemistry Services Specialized chemistry solutions provider offering process development, GMP manufacturing, flow chemistry, custom peptide synthesis, complex synthetics, and reactor build and design services using advanced software and equipment for biopharmaceutical clients.
  • Q1 Scientific Stability Storage Stability storage and sample management company providing pharmaceutical storage conditions meeting ICH Q1A requirements through walk-in and reach-in chambers for pharmaceutical and medical device companies.

Quantifiable outcome

  • Process mass intensity reduced by approximately 80% in organocatalytic process for obicetrapib
  • +4 more outcomes

Companies that use Cambrex

Customer profile

Named customers4 records

Segments4 records

Ideal customer profiles3 records

Cambrex technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

AI capability6 records

Feature7 records

Cambrex partnerships and signals

Strategic signal

Partnerships

Six partnerships are on record, tiered core and minor.

  • NewAmsterdam PharmacoreStrategic or Co-development Partner · 7 July 2026Collaboration on development of sustainable organocatalytic process for obicetrapib, resulting in American Chemical Society Green Chemistry Challenge Award. Achieved 80% PMI reduction, 70% cycle time reduction, and 50% cost reduction in manufacturing.
  • Alexion PharmaceuticalscoreStrategic or Co-development PartnerTechnology transfer and process development collaboration for danicopan, a complement Factor D inhibitor for paroxysmal nocturnal hemoglobinuria. Included significant process improvements in yield, PMI, and cycle times.
  • Q1 ScientificcoreOEM/ Whitelabel/ Licensing PartnerCambrex company providing stability storage and sample management capabilities. Q1 Scientific offers pharmaceutical storage conditions meeting ICH Q1A requirements through walk-in and reach-in chambers.
  • FlogasminorOthersCorporate Power Purchase Agreement (CPPA) partnership through Q1 Scientific to source renewable electricity from Cronalaght Wind Farm, covering approximately 50% of Waterford site electricity demand.
  • Snapdragon ChemistrycoreOEM/ Whitelabel/ Licensing PartnerAcquired by Cambrex, Snapdragon operates as a Cambrex company specializing in process development, continuous flow chemistry, and advanced manufacturing technologies including Z-Flow LPPS.
  • SanoficoreStrategic or Co-development PartnerCo-authored study on RIPK1 inhibitor oditrasertib demonstrating continuous flow manufacturing process for pharmaceutical production.

Scale indicators9 records

Recent moves6 records

Expansion highlights6 records

Cambrex competitors and assessment

Company assessment

Direct peers

  • Lonza Group: Global CDMO offering drug substance and drug product services across small molecules, peptides, and biologics. Most directly comparable to Cambrex as a leading one-stop-shop CDMO serving pharma and biotech customers.
  • Catalent: Major CDMO with drug substance, drug product, and clinical supply capabilities. Comparable to Cambrex in providing integrated development and manufacturing services to large pharma and biotech clients.
  • Siegfried Holding: Swiss-based CDMO specializing in small-molecule API manufacturing and drug product services. Highly comparable to Cambrex's custom API, generic API, and oral solid dose drug product offerings.
  • Recipharm: European CDMO with API and drug product manufacturing capabilities. Comparable to Cambrex as a mid-sized CDMO serving both innovator and generic pharma customers.
  • WuXi AppTec: Global CRO/CDMO with extensive small-molecule and biologics capabilities. A peer across the drug development and manufacturing value chain, particularly for biotech customers.
  • Bachem: Specialist CDMO in peptide and oligonucleotide API manufacturing. Most directly comparable to Cambrex's peptide platform (Z-Flow LPPS) and incremental peptide capacity at Karlskoga.

Broad incumbents

  • Thermo Fisher Scientific (CDMO/Patheon): Through Patheon and its pharma services division, Thermo Fisher offers comprehensive CDMO services including API, drug product, and clinical supply. A scaled, diverse incumbent competing with Cambrex across drug substance and drug product.
  • Charles River Laboratories: Provides discovery, preclinical, and manufacturing services to pharma and biotech. Overlaps with Cambrex in analytical and drug substance support and competes for biotech development budgets.

Others

  • Eurofins Scientific: Global laboratory testing services provider with strong pharma/biopharma analytical and CMC testing capabilities. Comparable to Cambrex's analytical services and Q1 Scientific stability storage offerings.

Emerging players

  • Samsung Biologics: South Korea-based large-scale CDMO expanding from biologics into synthetic and oligonucleotide manufacturing. An emerging adjacency to Cambrex in the contract API manufacturing space.

Market position

Strengths4 records

Weaknesses4 records

Competitive moat5 records

Key risks5 records

Key highlights7 records

Customer concentration

Cambrex social profiles

Digital presence

Cambrex compliance and trust

Trust signal

Compliance15 records

Cambrex financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Cambrex leadership team

Management profile

Number of profiles

Profiles8 records

Cambrex subsidiaries and ownership

Company hierarchy

Subsidiaries2 records

Cambrex funding detail

Funding detail

Funding overview

Funding rounds

Investors

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

Cambrex M&A and investment

M&A and investment

M&A6 records

Investments

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

Frequently asked questions about Cambrex

What does Cambrex do?

Cambrex is a global contract development and manufacturing organization (CDMO) that develops and manufactures active pharmaceutical ingredients (APIs) and drug products for pharmaceutical and biotech clients. The company provides end-to-end drug substance services (custom and generic API development and manufacturing, peptides, HPAPIs, controlled substances, biocatalysis, continuous flow), drug product services (oral solid dose formulation and clinical trial manufacturing), and analytical services (method development, stability testing, microbiology) across facilities in North America and Europe.

Is Cambrex a public or private company?

Cambrex is a private company. It is classified as unknown and is currently operating.

When was Cambrex founded?

Cambrex was founded in 1980. It employs 1,001 to 5,000 people.

Where is Cambrex based?

Cambrex is headquartered in East Rutherford, United States, in the North America region.

How does Cambrex make money?

Five revenue lines are on record. Drug Substance Development and Manufacturing is the primary driver. The others are generic API Manufacturing, analytical Services, drug Product Services and stability Storage Services (via Q1 Scientific).

Who are Cambrex's main competitors?

Direct peers on record are Lonza Group, Catalent, Siegfried Holding, Recipharm, WuXi AppTec and Bachem. Broad incumbents are Thermo Fisher Scientific (CDMO/Patheon) and Charles River Laboratories. Eurofins Scientific is listed as an others. Samsung Biologics is listed as an emerging player.

Does Cambrex have an API?

No public API is recorded for Cambrex.

What industry is Cambrex in?

Cambrex's product category is Pharmaceutical Contract Development and Manufacturing (CDMO). Its primary akta.pro industry code is HLAGABAA, Small-Molecule API & Intermediates CDMO, with a secondary code of HLAGABAB, Small-Molecule Drug Product (Solid/Oral/Parenteral) CDMO. Its NAICS code is 325411 and its SIC code is 2834.

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Live signals
GlobalDataCDMOs invest in European API capabilities to balance changing demand and supply chain risks, says GlobalData – GlobalDataCDMOs are expanding API capacity in Europe, with four investments between July and August 2026. Bachem plans to invest over CHF500 million in a Swiss facility, while Cambrex, Théa Group, and Merck also announced projects. The investments aim to meet demand for complex medicines and reduce supply chain risks.PR NewswireCambrex High Point achève les inspections préalables à l'autorisation menées par la FDA, la PMDA et la TGA, renforçant ainsi ses capacités de production commercialeCambrex announced on August 25, 2026 that it successfully completed three pre-authorization inspections at its High Point, North Carolina site, conducted by the US FDA, Japan's PMDA and Australia's TGA. The inspections enable the site to manufacture approved active pharmaceutical ingredients for the US, Japan and Australia, making it the company's last commercial production site. The site was expanded in 2023 for $38 million.Third NewsCambrex High Point Achieves Regulatory Milestones to Expand Manufacturing Capacity for PharmaceuticalsCambrex reported completing three Pre-Approval Inspections at its High Point, North Carolina facility, conducted by the U.S. FDA, Japan's PMDA and Australia's TGA, clearing it to manufacture approved active pharmaceutical ingredients for those markets. The site, expanded with $38 million in 2023, now has reactors up to 2,000 liters. No financial terms were disclosed.FinanzNachrichten.deEQS-News: Cambrex High Point schließt die Inspektionen im Vorfeld der Zulassung durch die FDA, die PMDA und die TGA ab und baut damit seine Kapazitäten für die kommerzielle Produktion weiter ausCambrex announced on 25 August 2026 that its High Point, North Carolina facility successfully completed pre-approval inspections by the US FDA, Japan's PMDA and Australia's TGA. The site, expanded in 2023 by $38 million, will produce approved APIs for the three markets and supports smaller-scale commercial production including orphan drugs.PR Newswire APACCambrex High Point Completes FDA, PMDA and TGA Pre-Approval Inspections, Advancing Commercial Manufacturing CapabilitiesCambrex announced on August 25, 2026 that its High Point, North Carolina facility passed Pre-Approval Inspections from the FDA, Japan's PMDA and Australia's TGA, enabling commercial API manufacturing for the US, Japan and Australia. The site follows a $38 million expansion completed in 2023 adding reactors up to 2,000 liters.PR NewswireCambrex High Point Completes FDA, PMDA and TGA Pre-Approval Inspections, Advancing Commercial Manufacturing CapabilitiesCambrex completed FDA, PMDA, and TGA pre-approval inspections at its High Point, North Carolina facility, enabling commercial manufacturing of APIs for the US, Japan, and Australia. The milestone follows a $38 million expansion completed in 2023, which added analytical and chemical development laboratories and commercial manufacturing operations.NJBIZCambrex invests $30M in new Italy R&D facilityCambrex announced the construction of a new $30 million R&D facility at its existing site in Milan, Italy, to add advanced analytical and process development capabilities. The expansion is expected to be completed in the second half of 2027 and includes the acquisition of adjacent land for future growth. This investment complements the company's broader five-year, $100 million strategy aimed at expanding production capacity across North America and Europe.AijournCambrex Milan Celebrates 80th Anniversary with Construction of New $30 Million R&D FacilityCambrex has commenced construction on a new $30 million research and development facility at its Milan, Italy site to expand analytical and process R&D capabilities. The project, scheduled for completion in the second half of 2027, includes the acquisition of adjacent land to support future growth in small molecule therapies.Third NewsCambrex Milan Marks 80 Years of Excellence with New R&D Facility InvestmentCambrex has begun construction on a new R&D facility in Milan, Italy, with a $30 million investment, to enhance its capabilities in drug development for complex small molecule therapies. The expansion, scheduled for completion in 2027, aims to support ongoing growth and innovation in pharmaceutical manufacturing.PR Newswire APACCambrex Milan Celebrates 80th Anniversary with Construction of New $30 Million R&D FacilityCambrex has commenced construction on a new $30 million R&D facility at its Milan, Italy site, with completion expected in the second half of 2027. This investment aims to enhance advanced analytical development and process capabilities for small molecule therapies while reinforcing the company's capacity to meet rising demand for CDMO services.