Wyszukano: HyClone products (Cytiva)
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Purification Process Workflow - Products from Masterflex
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Proces oczyszczania + Pompy Pompy Pompy perystaltyczne Masterflex PuraLev® Levitronix Single-Use Pump Series Akcesoria do pomp odśrodkowych Bezimpulsowa głowica pompy jednorazowego użytku + Pompy Pompy Pompy perystaltyczne Masterflex PuraLev® Levi...
Streamlining Procurement and Inventory Management Leads to Increased Productivity
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Streamlining Procurement and Inventory Management Leads to Increased Productivity Twoja rola Twoje wyzwanie Nasze usługi serwisowe Zasoby O nas Skontaktuj się z nami Challenge In addition to planning a relocation to a new headquarters to accommoda...
Inventory System Streamlines Procurement for cGMP Drug Production Facility
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Inventory System Streamlines Procurement for cGMP Drug Production Facility Twoja rola Twoje wyzwanie Nasze usługi serwisowe Zasoby O nas Skontaktuj się z nami Challenge An unstable system for managing production supplies often leads to interruptio...
Lean Inventory Management Program Reduces Costs for Production Environment
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Lean Inventory Management Program Reduces Costs for Production Environment Twoja rola Twoje wyzwanie Nasze usługi serwisowe Zasoby O nas Skontaktuj się z nami Challenge The high costs of managing cleanroom consumables inventory were dragging down ...
Stability Testing of New Drug Substances and Products Q1A (R2)
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Stability Testing of New Drug Substances and Products Q1A (R2) Webinar Tuesday 26th October 2021 11:00 to 12:00 CEST (Berlin Paris Madrid) Register now! Email Alerts Free Registration Chat Area Certificate of attendance To improve the quality of t...
Stability Testing of New Drug Substances and Products Q1A (R2)
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Stability Testing of New Drug Substances and Products Q1A (R2) Webinar Tuesday 15th October 2019 11:00 to 12:00 CEST (Berlin Paris Madrid) PRESENTED IN ENGLISH Replay Email Alerts Free Registration Chat Area Certificate of attendance
The Safer Choice: Improving Safety in the Lab through product selection and usage
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The Safer Choice: Improving Safety in the Lab through product selection and usage Webinar Thursday 3rd February 2022 11:00 to 12:00 CET (Berlin Paris Madrid) Replay Email Alerts Free Registration Chat Area Certificate of attendance The Safer Choic...
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...
Regulatory Agencies and Approvals
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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 mAbs
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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
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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...
~~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...
~~Avantor Services Cell and Gene Therapy Success Sto~~
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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...
Upstream processing for mAbs
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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...
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...
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...
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