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West is pleased to announce the addition of Stevanato Group’s (SG) clean, sterilized, depyrogenated EZ-fill® glass vials in 2R, 6R and 10R sizes for 13mm and 20mm stoppers and seals to its Online Store. These ready-to-fill vials are a high-quality option for general pharmaceutical use.
Sterilized SG EZ-fill® vials produced by Ompi join the current set of smaller quantity Ready-to-Use quality component offerings that are available on West’s Online Store for compounding pharmacies. The complete product line offering now includes:
Products available in the West Online Store are easy to access and purchase:
We encourage our compounding pharmacy customers to check out the on-line ordering options in our Online Store.
NovaPure®, Envision™, FluroTec® and Flip-Off® are trademarks and registered trademarks of West Pharmaceutical Services, Inc., in the United States and other jurisdictions.
FluroTec® technology is licensed from Daikyo Seiko, Ltd.
Crystal Zenith® is a registered trademark of Daikyo Seiko, Ltd.
Crystal Zenith® technology is licensed from Daikyo Seiko, Ltd.
SG EZ-fill® is a registered trademark of NUOVA OMPI srl
Focused on meeting customer needs in different markets and regions, West offers two types of washed Ready-to-Sterilize (RS) rubber closures: Regional-Washed RS and Westar<sup>®</sup> RS.
Where is the product catalog? What is my item number? These questions are often asked by customers new to working with West. The problem with such questions when it comes to choosing primary drug packaging is both complex and simple: <em>people don’t choose the container closure system – rather, the choice is made by the properties of the drug product. In other words, the drug <span> </span>chooses the container.</em>
<p>On March 18, 2014, West CEO Don Morel was the keynote speaker for the Beacon of Hope dinner held to celebrate the United Way of the Kearney (Nebraska) Area’s 50th anniversary. More than 200 attendees were on hand to help celebrate, and to hear stories of West’ philanthropy, which included a $25,000 donation from West to help the United Way reach its 2014 campaign goal.</p>
Parenteral drugs that are moisture sensitive are produced in a lyophilized state to protect against product degradation caused by moisture. As a result, when considering the stability and shelf life of lyophilized drugs, the residual drug moisture content is critical. It is also a crucial component in the dossier submitted for regulatory filing, which begs the question: How shall the moisture level in the lyophilized drug product cake be maintained during the drug product’s shelf life?
Administration of cell therapy drug products requires the delivery of cell suspensions without loss of function or viability. Cells must be transferred aseptically from their original container closure system to the administration system by infusion. However, the common transfer practice of using needles and syringes to pierce vial stoppers to retrieve contents poses a risk, namely needle-stick injury to clinicians.
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