Votre recherche pour: Whatman products (Cytiva)
1 598 les résultats ont été trouvés
Ansell Guardian® - helps companies select the right PPE solution to improve safety, productivity and cost performance.
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Ansell Guardian® - helps companies select the right PPE solution to improve safety productivity and cost performance. Webinar Tuesday 29th September 2020 11:00 to 12:00 CEST (Berlin Paris Madrid) Replay Email Alerts Free Registration Chat Area Cer...
Ansell Guardian® - helps companies select the right PPE solution to improve safety, productivity and cost performance.
/cms/fr/ansell_guardian_ppe
Ansell Guardian® - helps companies select the right PPE solution to improve safety productivity and cost performance. Webinar Tuesday 29th September 2020 11:00 to 12:00 CEST (Berlin Paris Madrid) Replay Email Alerts Free Registration Chat Area Cer...
L’importance du rôle des pompes dans le développement et la production des vaccins
/cms/fr/tech-article-pumps-important-role-vaccine-development
L’importance du rôle des pompes dans le développement et la production des vaccins L’être humain fait face à une multitude de menaces sanitaires de la grippe saisonnière banale aux germes pathogènes plus agressifs entraînant des maladies telles qu...
L’importance du rôle des pompes dans le développement et la production des vaccins
/cms/nl/tech-article-pumps-important-role-vaccine-development
L’importance du rôle des pompes dans le développement et la production des vaccins L’être humain fait face à une multitude de menaces sanitaires de la grippe saisonnière banale aux germes pathogènes plus agressifs entraînant des maladies telles qu...
Final fill for vaccines
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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...
Final fill for mAbs
/cms/nl/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 recombinant proteins
/cms/nl/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...
Regulatory Agencies and Approvals
/cms/fr/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 and Approvals
/cms/nl/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 cell therapy
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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...
Continued research
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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 gene therapy
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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...
Upstream processing for microbial-based recombinant proteins
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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...
Final fill for recombinant proteins
/cms/fr/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...
Final fill for mAbs
/cms/fr/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...
Upstream processing for mAbs
/cms/fr/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...
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