Du Søgte efter: UVP ULTRA VIOLET PRODUCTS
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Regulatory Agencies and Approvals
/cms/tech-article-regulatory-agencies-and-approvals
Regulatory Agencies and Approvals ASCII: American Standard Code for Information Interchange method of encoding characters into 7 or 8 binary bits (typically 7 bits plus an 8th bit for parity). ANSI: The American National Standards Institute is a p...
Final fill for recombinant proteins
/cms/bioprocessing_recombinant_proteins_final_fill
Final fill for recombinant proteins Progressing from the drug substance to the final injectable drug product requires final packaging vials and stoppers that meet a number of quality requirements. To meet these requirements products must be prepar...
Upstream processing for cell therapy
/cms/bioprocessing_cell_therapy_upstream_processing
Upstream processing for cell therapy Compared to production volumes associated with other biologics (e.g. mAbs: 2000L to 10000L) cell therapy production volumes are more commonly between 1L to 10L. Even the quality parameters are different. Instea...
Microbial based recombinant proteins
/cms/bioprocessing_recombinant_proteins
Microbial based recombinant proteins A wide range of recombinant proteins is produced using microbial (E. coli or yeast) fermentation – often being the preferred production method to drive efficiencies in the production process and to be faster to...
Nyheder
/cms/production_news
Nyheder Produktionsmagasin 2023- 2024 Bredt udvalg af steriliserings-pakninger i farmakologisk kvalitet (dæksler lommer poser etc) fremstillet af Tyvek fra Keystone Focus: Production – 2022-2023 CES & Safety Application notes library Your source f...
Continued research
/cms/moving_forward_together_continued_research
Continued research Moving your research forward relies on the right products and planning precisely when and where needed. Avantor is your complete resource for everything you need to ensure optimized research workflows – from consumables instrume...
Final fill for mAbs
/cms/bioprocessing_mabs_final_fill
Final fill for mAbs Progressing from the drug substance to the final injectable drug product requires final packaging vials and stoppers that meet a number of quality requirements. To meet these requirements products must be prepared in an ISO Cla...
Final fill for vaccines
/cms/bioprocessing_vaccines_final_fill
Final fill for vaccines Progressing from the drug substance to the final injectable drug product requires final packaging vials and stoppers that meet a number of quality requirements. To meet these requirements products must be prepared in an ISO...
Molecular Diagnostic Case Study
/cms/molecular_diagnostic_case_study
Molecular Diagnostic Case Study Fast Track to Early Detection NEED A molecular diagnostic company with in vitro diagnostics (IVD) technology for rapid and early detection of a common form of cancer approached VWR to manufacture and support commerc...
Cryopreservation-Cryo-tubes-BRLSPCRYOCOMB-EN
/m-dk.vwr.com/da_DK/images/Cryopreservation-Cryo-tubes-BRLSPCRYOCOMB-EN.pdf
to protect your samples Everything you need Thermo Scientific Cold Storage Tubes and Accessories and decrease cost maximize storage space You can decrease the cost to store your samples by HALF simply by maximizing your storage space. The cost to ...
Understanding the critical roles of cGMP chemicals and single-use technologies in cell & gene therapy manufacturing
/cms/understanding_the_critical_roles
Understanding the critical roles of cGMP chemicals and single-use technologies in cell & gene therapy manufacturing Webinar On demand Replay Rapid developments in cell & gene therapy have resulted in recent product approvals bringing these transfo...
Upstream processing for mAbs
/cms/bioprocessing_mabs_upstream_processing
Upstream processing for mAbs Developing and manufacturing mAbs has moved away from a dependency on raw materials of animal origin. Our biochemical components and supplements are animal component-free to meet the needs of these applications. Produc...
Final fill for gene therapy
/cms/bioprocessing_gene_therapy_final_fill
Final fill for gene therapy To meet these requirements products must be prepared in an ISO Class 5 environment and meet USP71 USP85 and USP758 requirements to be sterile pyrogen-free and particulate-free. They must also be validated for use in sto...
Assays for final fill
/cms/final_fill_assay
Assays for final fill Control is influenced by aseptic procedures followed in the production environment and is adhered to by employee training gowning cleaning and environmental control. Process validation steps are followed to ensure an acceptab...
Upstream processing for microbial-based recombinant proteins
/cms/bioprocessing_recombinant_proteins_upstream_processing
Upstream processing for microbial-based recombinant proteins Using microbial fermentation for the development and manufacture of recombinant proteins keeps on showing advantages e.g for the expression of proteins that do not require post-translati...
Sampling Solutions
/cms/sampling_solutions
Sampling Solutions Exact Volume Sampling Solutionss New aseptic and accurate sampling solutions from Avantor designed for your high value critical samples are flexible and scalable while reducing contamination risk. What fluid handling solution ca...
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