
Biologic drug substance CDMO services
Products


Information
From pre-clinical development to commercial supply, Patheon by Thermo Fisher Scientific is an industry leader in the development and manufacture of mammalian cell culture drug substances. Patheon offers biotech and pharmaceutical companies the ability to pursue opportunities around the globe with a fully integrated network of facilities. These world-class cGMP sites feature USP and DSP processes and technologies that enable us to meet your preclinical, clinical, and commercial milestones and goals for even your most challenging projects. With unmatched flexibility, Patheon gives you access to a breadth of options and technical expertise in biologic drug substance that will transform your expectations for yields, time to market and costs and that is supported by sterile manufacturing, including aseptic filling and lyophilization. •Process and analytical development of mammalian cell culture drug substances •Clinical and commercial cGMP manufacturing via fed-...
Main Categories
BiopharmaceuticalsCustom ManufacturingFinished Dosage FormsPharmaceutical PackagingAPIs (Active Pharmaceutical Ingredients)Contract Services - Analytical & Lab ServicesPharmaceutical Machinery & Technology
Available In
OceaniaNorth America (USA, Canada)Middle East Region (e.g. UAE)Central America (e.g. Mexico)East Asia (e.g. China, Japan, Korea)Europe - EU countriesEurope - non EU (e.g. UK, Russia, ex-CIS countries)South America (e.g. Brazil, Colombia)South Asia (e.g. India, Pakistan, Sri Lanka)South East Asia (e.g. Thailand, Philippines, Singapore)
All Categories
BiopharmaceuticalsCustom ManufacturingFinished Dosage FormsInjectablesParenteralsPharmaceutical PackagingBiopharmaceuticals (general category)BiosimilarsToxicology / VirologyChromatographyMethod DevelopmentMethod ValidationQuality Control TestingStability TestingAntibodiesAnalytical MethodsProcess ValidationToxicology / VirologyAnalytical DevelopmentContract ManufacturingContract PackagingCool ChainLogistics and DistributionLyophilisationProduct CharacterizationClinical Trials Phase I to IVAPIs (Active Pharmaceutical Ingredients)Quality controlSterilizationPlatform technologiesProcess validationContract Services - Analytical & Lab ServicesFormulation developmentRegulatory AffairsBiomanufacturingCapacity challengesCHO and cell linesCMCDownstreamMonoclonal AntibodiesTech transfer and Scale upUpstreamViral ClearanceFilling/ Fill Finish & packagingBioreactors & FermentationPharmaceutical Machinery & TechnologyInjectable systems and componentsContract ServicesPen injectorsPrefillable syringeAuto-injectorContract ManufacturingSterile Injectables ManufacturingAseptic Contract ManufacturingRegulatory consulting services
Supplied From
United States
