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 ...

In February, engineer-procure-construct contractor CRB was in the final stages of construction on a new production facility for Grand River Aseptic Manufacturing (GRAM) in Grand Rapids, Mich. Process ...

Modern grocery store shelves are filled with shelf-stable packaged foods. Everything from vegetables to dairy and meat products can be prepackaged and stored without the need for refrigeration, making ...

Limited remote, continuous measurement and poor instrument/software interconnectivity impede manufacturing management (enterprise) system deployment and restrict the use of analytical results for real ...

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 ...

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 ...

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, ...

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 ...

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 ...

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 ...