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Small Molecules
Method Development and Validation
Pharmaceutical Manufacturing
Release Testing
Stability Testing
Medicinal Cannabis Services
Biologics
Cell Banks
Bio Process
Characterization of Biologics
Aseptic Fill and Finish
Medical Devices
Chemical and Physical Analysis
Microbiology and Sterility
Packaging and Seal integrity Testing
Biocompatibility
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Small Molecules
Method Development and Validation
Method Feasibility, Qualification and Validation
Method Transfer Studies
Pharmaceutical Manufacturing
Facility and Process Control
Watersystem Validation
Environmental Monitoring
Disinfectant Efficacy Studies
Cleaning (Reprocessing) Validations
Microbial Identifications
Aseptic Fill and Finish
Labelling and Packaging
Supporting Services
Batch release - QC and QP
Non-Aseptic Fill and Finish
Labelling and Packaging
Supporting Services
Batch release - QC and QP
Extractables and Leachables
QC Release Testing
Chemical Testing
Microbiological Testing
Container Closure Integrity Testing
Release Testing
Raw Materials - API and excipients
Chemical Testing
Microbiological Testing
Solid-state characterization of Raw Material & Drug Product
Finished Dosage Forms
Chemical Testing
Microbiological Testing
NMR Characterization and QC Testing
Import Testing
Stability Testing
Medicinal Cannabis Services
Biologics
Cell Banks
Cell-line Production and Storage
Cell-line Characterization
Bacterial
Genetic Stability
Purity
Mammalian and Insect
Viability and titer
Genetic Stability
Purity
Bio Process
Raw Materials
Process Optimization
Analytical profiling with advanced chemometrics
Single use Bioprocess components
Process Validation
Viral Clearance
Cleaning (Reprocessing) Validations
Residuals Testing and Process related impurities
Downstream derived impurities
Cell culture related impurities
Host Cell Impurities
Endotoxins
Characterization of Biologics
Physico-chemical and Biochemical characterization
Identity
Product related Substances
Impurities
Biological activity characterization
Biochemical assay
Cell-based assay
Stability Testing
Aseptic Fill and Finish
Labelling and Packaging
Supporting Services
Batch release - QC and QP
Medical Devices
Chemical and Physical Analysis
Shelf-Life and product stability Testing
Extractables and Leachables
Microbiology and Sterility
Watersystem Validation
Environmental Monitoring
Cleaning (Reprocessing) Validations
Packaging and Seal integrity Testing
Shelf-Life and product stability Testing
Container Closure Integrity Testing
Biocompatibility
Biocides
Biocidal Industry
Detergents and household products
Biopesticides Testing
About us
About Eurofins BioPharma Product Testing Netherlands
History
Vision, Mission and Values
Quality
Accreditations Eurofins PROXY Laboratories
Accreditations Eurofins MicroSafe Laboratories
Accreditations Eurofins Bactimm
Accreditations Eurofins Spinnovation Analytical
News & Events
Careers
Data Privacy Notice
Downloads
Certificates and Licenses
Sample Submission Forms
Terms and Conditions of Sales
Terms and Conditions of Purchase
Instrumentation List Netherlands
Service flyers
BioPharma Services Newsletter
Contact
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