The analysis of mineral and additional trace metal screening of medicinal and recreational cannabis, as well as related products, provides key labeling information. The analysis can be carried out at all stages of production to ensure product quality control and products that are free of toxic metals.

Contamination in our waterways, soil, air, and food from microplastics (1 μm to 5 mm in size) is gaining significant public interest due largely to its emergence as an environmental and potential human health threat.

Here we introduce TwistAmp® Liquid, a new PCR replacement format that makes RPA technology more amenable to a wide range of research applications.

The synthesis of active pharmaceutical ingredients (API) may require multiple reaction steps that produce undesirable reaction byproducts or utilize various solvents that have to be removed from the finished product.

Whether you’re investing in your first digital imaging system for gel and membrane imaging, upgrading existing equipment, or just going with what’s already installed in your laboratory, you’ll need to understand key technical specifications to get the most out of your imager.

This ion chromatographic approach to the analysis of polar pesticides offers the ability to include multiple analytes in a single injection without derivatization.

Today’s drug discovery strategies require candidate compounds to fail early and cheaply in the discovery stage, rather than late and expensively in the clinical phase. Testing compounds in physiologically relevant model systems and leveraging information from image-based screens are ways to focus on those compounds that give rise to the right phenotypic changes without undesirable effects on the system.

Lunatic accurately measures highly concentrated biologics in a dilution-free, accurate and high-throughput way.

In this case study, learn how a multinational pharmaceutical company has expanded data analytics capabilities for 5000 users, starting with a small group in R&D, to early clinical trials, clinical trial development, safety, regulatory, and more.

This paper outlines the requirements of 21 CFR Part 11 and Annex 11, and provides information on how LabVantage software supports customers in complying with the regulations.