Sterile drug product CDMO services

Sterile drug product CDMO services

Products
Sterile drug product CDMO services
Sterile drug product CDMO services

Information

Thermo Fisher Scientific's flexible aseptic manufacturing and sterile fill finish solutions for your molecule's unique needs and challenges will enable success in early development, late-phase, and commercial manufacturing. Thermo Fisher offers extensive sterile product development and commercial manufacturing capabilities, including world-class expertise in lyophilization and ready-to-use dose formats.- Liquid small Volume Parenteral (SVP) - Liquid large Volume Parenteral (LVP) - Lyophilized Vial - Prefilled Syringes - Prefilled Cartridges- Autoinjectors and wearable devices
Main Categories
BiopharmaceuticalsFinished Dosage FormsPharmaceutical PackagingContract Services - Analytical & Lab ServicesPharmaceutical Machinery & Technology
Available In
OceaniaNorth America (USA, Canada)Middle East Region (e.g. UAE)East Asia (e.g. China, Japan, Korea)Europe - EU countriesEurope - non EU (e.g. UK, Russia, ex-CIS countries)South Asia (e.g. India, Pakistan, Sri Lanka)South East Asia (e.g. Thailand, Philippines, Singapore)
All Categories
BiopharmaceuticalsFinished Dosage FormsParenteralsPharmaceutical PackagingContract ManufacturingContract PackagingCool ChainLogistics and DistributionLyophilisationVial/ Syringe FillingDrug Formulation (general category)Aseptic technologyQuality controlSterilizationDrug Delivery Devices & SystemsVials / Cartridges / AmpoulesContract Services - Analytical & Lab ServicesFormulation developmentTech transfer and Scale upFilling/ Fill Finish & packagingPharmaceutical Machinery & TechnologyInjectable systems and componentsContract ServicesWearable devicePrefillable syringeAuto-injectorVial/syringe fillingSterile Injectables ManufacturingAseptic Contract Manufacturing
Thermo Fisher ScientificThermo Fisher Scientific provides industry-leading pharma services solutions for drug development, clinical trial logistics, and commercial manufacturing to customers through our Patheon brand. With more than 60 locations around the world, we provide integrated, end-to-end capabilities across all phases of development, including API, biologics, viral vectors, cGMP plasmids, formulation, clinical trials solutions, logistics services, and commercial manufacturing, and packaging. Built on a reputation for scientific and technical excellence, we provide pharma and biotech companies of all sizes instant access to a global network of facilities and experts across the Americas, Europe, Asia, and Australia. We offer integrated drug development and clinical services tailored to fit your drug development journey through our Patheon(TM) Quick to Care(TM) program. Our Patheon(TM) Quick to Clinic(TM) programs for large and small molecules help you balance speed and risk during early development so you can file your Investigational New Drug Application (IND) quickly and successfully. Digital innovations such as our mysupply Platform and Pharma 4.0 enablement offer real-time data and a streamlined experience. Together with our customers, we're rapidly turning pharmaceutical possibilities into realities.

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