Procurou por: Whatman products (Cytiva)

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 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...

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...

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 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 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...

Solon Manufacturing Facility Core Capabilities Manufacturing and supply of high-purity biochemicals reagents and custom services for life sciences Manufacturing quality control testing dispensing finishing assembly for regulated and non-regulated ...

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 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 Webinar On demand Replay Rapid developments in cell & gene therapy have resulted in recent product approvals bringing these transfo...

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...

Order Entry - How to Upload Do you maintain a list of products outside of the vwr.com web site? Do you wish you had a way to load your list into the Order Entry screen or Shopping Basket? Well here is the solution. The ~~Upload a List of Products~...

Laboratory Quality Manager Your Role Your Challenge Our Services Portfolio Resources About Us Contact Us Stay Compliant with Regulations Deadlines and Expectations The reputation of your laboratory rests on your shoulders. From the start of produc...

Final fill for cell therapy The cell therapy drug product is configured in different ways depending on the required delivery of the cells/tissues. For example delivery of chondrocytes for cartilage repair is administered by an injection. Expanded ...

Fine Chemicals from Alfa Aesar & Acros Organics The Acros Organics and Alfa Aesar brands provide an extensive range of chemicals, functional reagents, organic building blocks, metals and life science reagents for research and development and quali...

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...