mAbxience and Sandoz are targeting a $5.7 billion market with a proposed emicizumab biosimilar for hemophilia A.
|Podcasts|March 11, 2022
Powder Handling Challenges in Upstream Biopharmaceutical Processes
Author(s)ILC Dover
For years pharmaceutical and biopharmaceutical manufacturers have invested in rigid stainless-steel equipment for upstream bioprocessing. With new and innovative single-use products now on the market, manufacturers have access to flexible, safe solutions that offer a myriad of advantages over the traditional solutions. Single-use technology offers less risk of contamination, more operator safety, and less negative environmental impact than the stainless-steel alternatives. In this podcast, we will discuss the challenges associated with handling powders in upstream biopharm processes and how single-use technology can benefit manufacturers from an environmental, cost, and safety perspective.
Related to this article
Fayuvi scored 23.5 points higher than untreated peers on cognitive testing, backing the first-ever approval for a Sanfilippo syndrome A gene therapy.
Athenecia Faggins of Minaris Advanced Therapies discusses raw material qualification, supplier management, testing, and risk control for advanced therapy manufacturing.
FDA compliance officers detailed 2026 guidance updates, online drug sale enforcement, and a first-of-its-kind AI-related warning letter at the PDA/FDA Joint Regulatory Conference.
Sanofi’s Jack Prior discusses how biopharmaceutical manufacturers can assess whether process data is ready for human and AI use, and the role of data quality, accessibility, governance, and AI in manufacturing.
Panelists from FDA, Genentech, and Minaris discussed raw material risk, supplier oversight, and at-risk release strategies for advanced therapies at the PDA/FDA Joint Regulatory Conference.
Dualitas will screen over 300,000 bispecific combinations for Roche, backing a deal worth up to $1 billion in immunology research.
FDA's Francis R.W. Godwin (CDER) and Kathleen Jones, PhD (CBER) detail a record pace of drug warning letters and the CGMP deficiencies most commonly cited in biologics facility inspections.