Esta buscando: 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...
Regulatory Agencies
/store/externalContent/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...
Inventory System Str
/store/externalContent/avantor_services_success_stories_inventory_system_streamlines_procurement
Inventory System Streamlines Procurement for cGMP Drug Production Facility Your Role Your Challenge Our Services Portfolio Resources About Us Contact Us Challenge An unstable system for managing production supplies often leads to interruptions in ...
Life Science All You
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Life Science All You Need At VWR we enable Life Science throughout the world by providing the power of choice with over 5 million products for our customers. You will find new tools and products in the All You Need areas for the workflows of Cell ...
~~cGMP-Procurement-and-Supply-Management~~
/us.vwr.com/en_US/images/cGMP-Procurement-and-Supply-Management.pdf
continued on next page INVENTORY SYSTEM STREAMLINES PROCUREMENT FOR cGMP DRUG PRODUCTION FACILITY SUCCESS STORY cGMP Procurement and Supply Management Problem An unstable system for managing production supplies often led to interruptions in produc...
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...
Upstream processing for vaccines
/cms/bioprocessing_vaccines_upstream_processing
Upstream processing for vaccines Optimal production of vaccines is achieved in mammalian expression and insect systems using cell lines that are anchorage-dependent or suspension enabled. For most vaccines optimal production is achieved in mammali...
Protein production -
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Protein production - FectoPRO® The FectoPRO® Transfection Kit is specifically designed for enhanced Transient Gene Expression (TGE) in suspension CHO and HEK-293 cells in various serum-free media using low DNA amount (<1 μg/ml of cell culture). Am...
Avantor Services Cell and Gene Therapy Success Sto
/m-es.vwr.com/es_ES/images/Avantor_Services_Cell_and_Gene_Therapy_Success_Sto.pdf
Success story Avantor accelerates Cell and Gene Therapy (C>) production Avantor Services Lab and production services CHALLENGE A global pharmaceutical company set an ambitious strategic goal of transitioning from Cell and Gene Therapy (C>) con...
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...
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...
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...
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...
~~cgmp procurement and supply management eu~~
/m-mx.vwr.com/es_MX/images/cgmp_procurement_and_supply_management_eu.pdf
Problem The challenge of managing inventory created unnecessary costs depleted manufacturing time and exposed an FDA-certified facility to the risk of shutdown. Solution VWRCATALYST implemented an inventory system to manage the efficient delivery ...
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...
Accelerate cGMP Prod
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Accelerate cGMP Production Processes Your Role Your Challenge Our Services Portfolio Resources About Us Contact Us Exceed cGMP Standards in Your Operation Increase efficiency. Reduce costs. Focus on profitability. It’s the mantra echoing through t...
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