Sterilin non-pyrogenic polystyrene containers are certified endotoxin-free to levels below 0.01EU/ml, making them ideal for use in the pharmaceutical industry for the storage of samples, formulation work, sterility testing and endotoxin testing. Sterilized by gamma irradiation, they are available in a wide range of volumes.
Sterilin non-pyrogenic polystyrene containers are certified free from endotoxins to levels below 0.01EU/ml, with the test procedure validated according to EU, USP and USFDA guidelines. This enables them to be used with confidence in a wide variety of applications within the pharmaceutical industry, including sample storage, formulation work and sterility testing, as well as endotoxin testing.
These high quality Sterilin non-pyrogenic containers are manufactured from virgin polystyrene to ensure excellent quality and clarity. All materials are non-cytotoxic and the containers are sterilized by gamma irradiation.Sterilin non-pyrogenic containers are available in a wide range of sizes, from Bijou (7ml) and Universal (30ml) up to 250ml capacity. They are supplied with the lot number printed on each container label and with leak-free caps (leak tested in accordance with EN14254 Annex D) to prevent the loss of hazardous or valuable contents. In addition, a test certificate, that demonstrates the containers do not inhibit or enhance the LAL (Limulus Amoebocyte Lysate) test, is available for each lot.
For more information click here.
Sterilin is part of Thermo Fisher Scientific.
Why is the PDA Pharmaceutical Microbiology Conference the Hottest Ticket in the Industry?
October 10th 2024Get a glimpse of the power and popularity behind the PDA Pharmaceutical Microbiology Conference from two planning committee members, Julia Marre, PhD (Associate Director, Scientific and Regulatory Affairs at Pocket Naloxone Corp) and Dawn Watson (Executive Director, Global Micro Quality and Sterility Assurance at Merck). This candid conversation reveals why this industry event is so influential…and always sold out! The speakers discuss what makes the PDA Pharmaceutical Microbiology Conference so vital to industry professionals, as well as how to become a part of this dynamic professional community.
Navigating Annex 1 for Early Phase Sterile Fill Finish in Clinical Supplies
November 21st 2024Stay compliant with Annex 1 for early phase sterile fill finish processes. Discover how to implement robust contamination control strategies, integrate isolator technology, and conduct integrity testing to meet stringent European Union standards. The guide provides a comprehensive look at key elements such as PUPSIT, critical zone controls, and monitoring and training for aseptic processes.
Your Ultimate Guide for CMC Testing Support for Gene and Cell Therapy
November 21st 2024Explore the complexities of gene and cell therapy development with our comprehensive guide to Chemistry, Manufacturing, and Controls (CMC) testing. Learn how our expertise ensures the safety, potency, and quality of advanced therapies, supporting your journey from product development through regulatory approval.