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GMP Flow Cytometry: Applications, Considerations and Challenges

This webcast features: Jamie Hall, Project Manager, Center of Excellence for Biopharmaceuticals, Intertek Pharmaceutical Services Flow cytometry is a powerful technique which can be applied to all stages of the drug development pipeline including discovery, clinical development, CMC, regulatory submission and in support of production. It allows the analysis of complex mixtures of particles, from polystyrene beads to cells. Utilizing a broad spectrum of fluorescent detectors, assays can be set up to assess multiple parameters at once and ascertain otherwise…

China’s GMP Strategies: Dealing with Quality Management Issues, to Compete with the West

This webcast features: Dr. Fai Poon, President, Quacell Biotech Ltd. China’s biopharma sector faces multiple challenges in quality management, including lack of experience and talent, a rapidly changing regulatory environment, as well as cultural issues in management. In Part 3 of our series Fai Poon, President, QuaCell Biotech, Ltd., will cover China regulatory issues, a review of current challenges in biopharma quality management in China, and opportunities for progress in this field with the growing CMO platforms and the emerging…

Rapid Process Optimization with Customizable Single-Use Bioreactors: The Bioreactor That Adapts to Your Bioprocess

To enhance their performance, life science specialists require flexibility in their work and tools. The increasing diversity of bioprocess applications calls for different cultivation methods. Therefore, being able to customize processes and equipment is a significant advantage. With over 45 years of experience in customizable multi-use bioreactors, Applikon Biotechnology now provides the same flexibility with customizable single-use bioreactors. The AppliFlex ST bioreactor is a fully configurable, stirred-tank, single-use bioreactor that can be designed to specific customer demands. Using three-dimensional (3D)…

Advancing Robust Manufacture of T-Cell Therapies: Application of Single-Use Stir-Tank Bioreactors

With the increase of T-cell immunotherapy research, cell therapy developers have encountered the difficulty of producing consistent, high-quality products. Approved therapies Kymriah™ (tisagenlecleucel, Novartis), Yescarta™ (axicabtagene ciloleucel, Kite Pharma), and late-phase clinical products BB2121 and UCART19 have been critiqued for presenting potential obstacles to patient access because of high costs of treatment and variable manufacturing outcomes. Manufacturing processes need to be developed to increase control over each unit step in a way that improves product consistency over the life of…

Eppendorf BioBLU® 10c Single-Use Vessels Simplify Handling of Cell Culture Bioprocesses at Bench Scale

Substituting traditional glass bioreactors with single-use equipment can simplify a bioprocess workflow. Implementing single-use vessels eliminates the need for cleaning and autoclaving, thus reducing the time needed to prepare a bioprocess run and lowering contamination risk. Another advantage is that single-use vessels reduce occupational hazards associated with overweight handling (especially at larger bench scales) because plastic weighs less than glass. Fill out the form below to read the complete white paper now.

Updating Biologics Manufacturing: Using Modern, Single-Use Powder Handling Reduces Time to Market and the Chance of Contamination

Biopharmaceutical companies are striving to produce biologics more efficiently with a lower cost point and fewer employees. Most small-scale media and buffer operations are carried out with small bottles of liquid media. But as processes are scaled up to manufacturing levels, that is no longer a viable option. Costs of shipping liquid are simply prohibitive, so the industry has migrated to using media and buffers in powder form. In fact, 90% of cell culture media and buffers for sale is…

Increase Viable Sf9 Cell Density and Baculovirus-Based VLP Production by Supplementation with Recombinant Insulin Human AF

Virus-like particles (VLPs) have become a promising means for developing vaccines and gene therapies. Currently, vaccines based on VLPs are commercially available for human papillomavirus and hepatitis B and E. Other disease treatments with VLPs are undergoing clinical trials. Upon expression, the structural matrix polyprotein group-specific antigen (gag polyprotein) from the human immunodeficiency virus (HIV) has shown to accumulate beneath the lipidic membrane. After a sufficient number of gag polyproteins are recruited, the assembly process is finished, and the VLP…

New Single-Use Bioreactor for Cellular Products of Consistent Quality: BIOSTAT® RM TX Bioreactor with Flexsafe® RM TX Bags

Sartorius Stedim Biotech (SSB), a leading international supplier for the biopharmaceutical industry, has launched the BIOSTAT® RM TX single-use bioreactor, a new wave-action mixer system developed specifically for closed, automated expansion of consistent-quality cell therapies such as ex vivo cellular immunotherapies. This new good manufacturing practice (GMP) platform combines SSB’s established single-use Flexsafe® bag technology with the company’s expertise in biopharmaceutical automation. Fill out the form below to read the complete technology review.

Cell Culture Expansion in Fully Closed Erlenmeyer Shake Flasks Outside the Biosafety Cabinet

Expansion of suspension cell culture from cell bank to bioreactor is performed through passages of successively larger Erlenmeyer shake flasks. A traditional cap must be unscrewed for each fluid transfer. Risk of contamination is mitigated by performing these fluid transfers in a biosafety cabinet (BSC) or laminar flow hood. Work in a BSC is not preferred because of high maintenance and operating costs, intensive cleaning and decontamination procedures, and the inconvenience of performing operations in the BSC. Despite the use…

New Approach for Qualifying Liquid Handling in Single-Use Bags

2D Flexsafe® Bags and Shells Offer Strong Validation: Complete logistical solution for handling and shipping of liquid bulk drug substance in a 2D Flexsafe® bag & shell Quality by design principles Comprehensive and innovative testing program following the guidelines like ASTM, NF and ISO The system allows for safe variable shipping volumes of 10–120% of nominal fill volume and can be leveraged by the end-users for their own process validation Fill out the form below to view the complete poster…