This product is not clubbable with other items in cart. Please remove this or other items to proceed further.
No Items In Cart
Pharmaceutical closures used in aseptic environments must be introduced in a sterile state. The most common methods to sterilize rubber closures (e.g., stoppers) are autoclaving (saturated steam) and gamma irradiation. Both methods can influence chemical (e.g., extractables profile) and physical/functional properties (e.g., break-loose and extrusion forces). Therefore, it is important to choose the right method.
To meet the diverse needs of customers, West offers a broad portfolio of rubber stoppers and plungers, as either:
For Westar RU sterile components, assurance is to a sterility level (SAL) of 10-6 or better, i.e., probability of microbial contamination is no greater than one component per one million (Guidance for Industry: Container Closure System Integrity Testing Lieu of Sterility Testing as a Component of the Stability Protocol for Sterile Products – https://www.fda.gov/RegulatoryInformation/Guidances/ucm146074.htm)
Westar RS components must be sterilized by the pharmaceutical company. West typically recommends autoclaving: (a) a steam cycle at a minimum temperature of 121.1°C (not to exceed 123°C) for a maximum of 60 minutes, followed by (b) a drying cycle at 105°C for a maximum of 8 hours. For select applications, gamma irradiation may be the right choice. Whatever method is used, the pharmaceutical company must ensure that sterilized components meets sterility and compendial standards (USP <381> and EP 3.2.9).
West Technical Customer Support can assist in selecting the right sterilization method, and in collaboration with Analytical Laboratory Services, to perform compendial tests.
STERIlizableBAG™ and Westar® are registered trademarks or trademarks of West Pharmaceutical Services, Inc. in the United States and other jurisdictions.
Take an in-depth look at the science behind containment & delivery of injectable medicines in the West Knowledge Center.