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In aseptic pharmaceutical manufacturing, the packaging for parenteral packaging components is essential for ensuring proper sterilization and utilization. The importance cannot be overstated. Ineffective component packaging can potentially affect patient safety, and result in significant financial loss. Acknowledging this, West conducts exhaustive testing on its packaging systems to ensure that quality and functionality requirements are achieved.
Ensuring the sterility of medicinal products has always been one of the key concerns of drug manufacturers, due to the dire health implications it could have on patients, as well as the potential for costly product recalls. The importance of control strategies to ensure drug products remain sterile has also been reiterated recently by regulatory agencies such as the U.S. Food and Drug Administration (FDA) and The European Medicines Agency (EMA) in their respective guidelines:<br /><ul><li>FDA: Sterile Drug Products Produced by Aseptic Processing – Current Good Manufacturing Practice</li><li>EU GMP Annex 1 Manufacture of Sterile Medicinal Products</li></ul>
Employees at West’s Eschweiler, Germany, facility celebrated the holidays with a party that had some very generous results. The party took place on December 15, 2012, with more than 520 employees attending and participating in a lottery for three superb prizes, including a flat-screen television, digital camera and gift voucher for gas.
West Pharmaceutical Services Brazil is pleased to host the VII Technical Symposium on October 28, 2014, at the Melia Hotel Jardim Europa in Sao Paulo, Brazil.
It’s spring and West technical experts are out and about visiting and presenting at tradeshows near and far.
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