Western pharm los angeles

Designed to meet the highest standards West NovaPure® stoppers are consistent, reliable, high-quality components based on clean, modern elastomer formulations. Developed under Quality by Design principles, NovaPure stoppers meet patient needs and mitigate risk.

Enhanced Pharmaceutical Components Daikyo Ready-to-Use-Validated (RUV)® and Ready-to-Sterilize-Validated (RSV)® components are manufactured using clean, high-quality elastomer formulations that are washed and sterilized to help reduce the manufacturing footprint, streamline processes, outsource risks around component preparation, and reduce bioburden associated with aging facilities and inflexible plant layouts.

• Size2ml and 5ml

One source. One system. One solution. The West Ready Pack® system is comprised of high-quality primary and secondary packaging components. The Ready Pack system consists of sterilized NovaPure® stoppers, Flip-Off® seals, vials and vial adapters. Ready Pack system components are provided ready to use with available sterilization validation summaries to help you minimize internal processing upon receipt. With small quantity availability, the Ready Pack system is particularly suited for R&D purposes or small filling operations.

Flexible solutions for pharmaceutical components Westar® Ready-to-Use (RU) or Ready-to-Sterilize (RS) stoppers can help streamline preparation and deliver a consistent product for use in fill-finish operations.

Stick to Your Schedule, Not Your Shelves™ West LyoTec® stoppers have West FluroTec® film applied to their top surface, which helps eliminate stoppers from sticking to pressure plates and reduces stopper clumping in sterilizers and feeding bowls. Stopper performance in the lyophilization chamber is critical, whether processing is done in the pharmaceutical manufacturer's facility or at a contractor’s site.

An Investment in Drug Purity West FluroTec® barrier film is your premier choice to protect drugs from contamination by providing an effective barrier minimizing interaction between the drug and the closure while maintaining container closure integrity.