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Procurou por: CENTURION SAFETY PRODUCTS

631  resultados encontrados

Ciência avançada de baterias - Gestão de instalações e proteção

Ciência avançada de baterias - Gestão de instalações e proteção A Avantor está a colocar em movimento a ciência das baterias para criar um mundo melhor Avantor tem uma vasta gama de produtos para manter as instalações seguras limpas e organizadas....

AP A9019 qPCR Mycoplasma Test Kit

1 qPCR Mycoplasma Test Kit Real time/qPCR test kit for mycoplasma detection Product code A9019___________________________________________________________________________ j Description The Mycoplasma PCR Detection Kit is based on a 5-Nuclease probe...

Valve Selection Guide

Valve Selection Guide Valve Terms Breaking Pressure: The minimum pressure required to produce flow through a valve. Duty Cycle: 100% duty cycle is defined as continuous operation without any damage occurring. For intermittent duty cycle (<100%) al...

Hearing Fit Testing

Hearing Fit Testing Using Fit Validation to Help Improve Field Performance of Hearing Protectors and increase Compliance The chosen hearing protector (earplug or earmuff) won’t provide the expected level of protection if it is not fitted or used c...

Final fill for vaccines

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...

Avantor Services Cell and Gene Therapy Success Sto

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 cell therapy

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 recombinant proteins

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 microbial-based recombinant proteins

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...

Upstream processing for mAbs

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...

Assays for final fill

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...

Final fill for mAbs

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...

Novel Single-use Solutions for Cell & Gene Therapy Manufacturing

Novel Single-use Solutions for Cell & Gene Therapy Manufacturing Webinar On demand Replay As cell and gene therapies offer patients the promise of transformative treatments for challenging diseases it’s vital to innovate and accelerate the process...

Designing Novel Fluid Sampling Systems for GMP Operations

Designing Novel Fluid Sampling Systems for GMP Operations Webinar On demand Replay Sampling is a requirement in every process step of biopharmaceutical manufacturing with an increasing demand on accuracy the closer it comes to final finish. The we...

Final fill for gene therapy

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...

Understanding the critical roles of cGMP chemicals and single-use technologies in cell & gene therapy manufacturing

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...
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