Lonza

global GMP capacity (Lonza Visp/US, Catalent, Thermo Fisher Patheon) that lets a sponsor manufacture in-region without owning a plant.

Country
Switzerland
Commercial Pure-Play CDMO
Coverage
CNEUINUS
analytics-pat
cleanroom-facilities
consumables
market-access-commercial
therapeutics-platforms
Regulatorsfdaemanmpa

Verifiable facts

FactValueSource
RevenueCHF 6.5 billion for FY 2025lonza.com
Capacitytotal bioreactor capacity of around 332,000 liters (including Vacaville site)lonza.com · pharmamanufacturing.com
Capacitysingle-use bioreactor technologies up to 2,000L and stainless-steel bioreactors from 6,000L to 25,000Llonza.com
CertificationcGMP-compliant facilitieslonza.com
Regulatory approval80+ successful site inspections by 14 global health authorities (including FDA and EMA) in last 5+ yearslonza.com
Production site6-7 cGMP manufacturing sites globally (across three continents)lonza.com
Headcount20,000 colleagueslonza.com
HeadquartersBasel, Switzerlandlonza.com

Independent sources: pharmamanufacturing.com

Technologies
NameClusterRisk
Bioproduction CDMO/CMO (biologics/ATMP/mRNA)therapeutics-platformsLow
Chemoenzymatic API synthesis (biocatalytic small-molecule manufacturing)therapeutics-platformsLow
Endotoxin testing systemsanalytics-patLow
Local manufacturing for market accessmarket-access-commercialLow
Media manufacturing (B2B production equipment)cleanroom-facilitiesLow
Microcarriers for adherent cell culturesconsumablesLow

Compiled by BIOECON from primary sources.

Compliance Bioecon is an information intermediary; it is not a regulator, a certification body, or a legal advisor. When working with public-sector customers (procurement under 44-FZ / 223-FZ), Bioecon acts solely as an independent analytical platform, with no remuneration from suppliers.