Aseptic processing improvements aim to reduce contamination from operators, yet interventions remain necessary, increasing contamination risk. 'Inherent' and 'corrective' interventions are ...
Dublin, April 15, 2026 (GLOBE NEWSWIRE)-- The "Mastering Aseptic Processing for Pharmaceutical & Biotech Manufacturing (Mar 24th - Mar 25th, 2026)" training has been added to ResearchAndMarkets.com's ...
Dublin, July 28, 2025 (GLOBE NEWSWIRE) -- The "Aseptic Processing and Validation Course - FDA Expectations and Industry Best Practices" has been added to ResearchAndMarkets.com's offering. Aseptic ...
AGAWAM, Mass., July 31, 2012 /PRNewswire/ -- An unscheduled inspection of an aseptic manufacturing process can hit a pharmaceutical company with the fury of a New England nor'easter. But a new ...
According to the National Cancer Institute, immunotherapies that enlist and strengthen the power of a patient’s immune system are the “fifth pillar” of cancer treatment adding to surgery, chemotherapy ...
Sterile products may be broadly classified into two main categories based on their production mode -- those that are terminally sterilized following the filling and sealing of the container and those ...
Limited remote, continuous measurement and poor instrument/software interconnectivity impede manufacturing management (enterprise) system deployment and restrict the use of analytical results for real ...
To assure patient safety, biologics developers and manufacturers must carefully consider where contaminants could be introduced to the drug substances (DSs) or drug products (DPs) at all stages of the ...
Why is aseptic processing important in pharmaceutical manufacturing? The manufacturing of both sterile drugs and biological products can be achieved through terminal sterilization or aseptic ...
When it comes to keeping it clean, Philip Nelson delivers. As a professor of food science at Purdue University, he spent years perfecting the primary method that today allows many juices and other ...
An interview with Gilberto Dalmaso, discussing the different grades of pharmaceutical cleanrooms and the production of high-level compounds under aseptic conditions. Please give an overview of ...
The US Food and Drug Administration (FDA) last week warned Japanese drugmaker Takeda Pharmaceutical over good manufacturing practice (GMP) violations observed during an inspection of its Hikari, ...
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