Insilica's Dr Thomas Luechtefeld argues process traceability, not benchmark accuracy alone, determines whether AI toxicology decisions can be trusted.
|Articles|May 1, 2014
- BioPharm International-05-01-2014
- Volume 27
- Issue 5
Aseptic Valve Range Increases Sterility
Aseptic Valve Range Increases Sterility
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ChargePoint AseptiSafe by ChargePoint Technology is designed to transport aseptic products or components. The valve range consists of two iterations capable of eliminating the ‘Ring of Concern’ through different methods to achieve sterility. ChargePoint AseptiSafe uses a steam-in-place process that ensures the sterilization of the internal surfaces of the valve together with the Ring of Concern. In addition, ChargePoint Aseptisafe bio uses a fast gassing system that sterilizes the valve interface in approximately six minutes.
Articles in this issue
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Accelerated Stability Modelingover 12 years ago
Demand for New Vaccines Spurs Innovationover 12 years ago
Standardizing Practices for Disposablesover 12 years ago
Clinical Syringe Packages Increase Productivityover 12 years ago
Linking Drug Shortages and Quality Metricsover 12 years ago
Improving Protein Expression with Novel Systemsover 12 years ago
Integrated Single-Use Sterile and SIP Connector Provide Flexibilityover 12 years ago
India's Developing Market Offers OpportunitiesAdvertisement
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Nate Edwards of Arya Consulting moderates a discussion with Elisabeth Gardiner of Tevard Biosciences and Donny Xu of the RTW Institute about the regulatory and manufacturing hurdles facing rare disease drug developers.
Rohit Tripathi, vice president of industry strategy, consumer packaged goods, and manufacturing at RELEX Solutions, explains where cold-chain planning still breaks down and why biopharma supply chain leaders should use AI to act on data sooner, with humans making the final call.
Zylidac will test whether optogenetic cell lines that hit 21 g/L in small-scale CHO runs can deliver higher-yield complex biologics at GMP scale.
Revakinagene taroretcel (Encelto), the only FDA-approved MacTel therapy, slowed photoreceptor loss by up to 54.8% vs sham in phase 3 trials.
Rohit Tripathi, vice president of industry strategy, consumer packaged goods, and manufacturing at RELEX Solutions, explains what is driving biopharma reshoring, how USMCA uncertainty complicates sourcing for biologics, and where cold-chain visibility still breaks down.
Backed by €400 million (US$449 million) in EU-cleared German aid, the new Frankfurt facility is designed to secure insulin supply for people with diabetes from 2032.
EA2251, the 7th registrational trial of ivonescimab, will test it plus chemotherapy vs pembrolizumab or durvalumab regimens in first-line BTC.
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