Traditional endotoxin testing has long had pain points including analyst subjectivity, extensive training requirements, and the potential for data integrity violations. An invalid test can result in lengthy investigations, costly retests, and the risk of an FDA finding or audit, possibly crippling your manufacturing timelines.While LAL is the most sensitive and
The newest issue of Neogen’s Insider Magazine is out! This time focusing on hygiene, a crucial element for any organisation in the food industry.Take a look at the science behind ATP hygiene monitoring systems and find out why Neogen’s AccuPoint® Advanced is the only ATP system validated by AOAC.
Why stick to traditional media plates if there is an alternative which can improve your workflow, while providing accurate and reliable results? Our new MC Media pads for microbial testing are small to save you space in storage and in the incubator.Simply inoculate by adding your sample – no spreading required – then
QC professionals know that data integrity and its practical maintenance are crucial for the quality of products and safety of patients. But how does it apply to endotoxin testing?Our webinar archive, “The Importance of Data Integrity for Endotoxin Testing” is available for viewing in our QC Insider™ Toolbox. Our support tool
What makes Puritan® standout from the rest? It’s our unique, multi-length flock fiber technology that sets our HydraFlock® and PurFlock Ultra® apart from the rest.The ultra-effective collection and elution properties of our flock will make your job easier and you’ll get better results — even with the smallest of samples.
12 – 14 June 2018Lonza invites you to attend the 4th Endotoxin Testing Summit 2018, a vivid platform to:- Network with QC directors, lab managers, key opinion leaders, users and regulators
- Gain insight into hot topics, such as overcoming data integrity, low endotoxin recovery (LER), new regulatory guidelines, and novel endotoxin testing approaches
Neogen’s range of validated rapid and conventional testing solutions can simplify the Listeria workflow of your microbiological testing laboratory.Choose From:- Rapid plating method offering greater sensitivity than ISO 11290-1: One Broth One Plate- Analysis of environmental samples within 60 minutes with no enrichment required: Listeria Right Now™- Cost saving
When it comes to patient safety, should close enough ever be good enough? In an industry that relies on cutting edge technology to stay compliant, a subjective, visual final sterility confirmation is no longer acceptable.Celsis® rapid microbial detection takes the guesswork out of determining your product’s sterility by providing a
Using intelligent imaging, the APAS Independence can consistently screen and sort 200 plates per hour and quickly remove negative plates out of the workflow.The innovative triage system uses sophisticated machine learning algorithms built on input from real microbiologists, as well as expert rules based on international guidelines.
12 – 14 June 2018 - Register before 31 April for a 200 USD savingLonza invites you to attend the 4th Endotoxin Testing Summit 2018, a vivid platform to:- Network with QC directors, lab managers, key opinion leaders, users and regulators
- Gain insight into hot topics, such as overcoming low endotoxin recovery (LER), data integrity, new regulatory
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