This presentation will provide an insight into baseline correction, spectral bandwidth, data interval, and many additional settings

This presentation covers the basics of adapting the dissolution environment for low-dose, extended-release dosage forms (e.g., medical devices).

We will discuss factors affecting peak shape, such as the column, sample, mobile phase, and more, and offer remedies for improving peak shape.

Development through the integration with selected QbD software that enables the required DoE approach.

LCTech's specialized equipment designed to optimize each step of the dioxin workflow, ensuring efficient processing, high-quality data, and safety.

Learn about the capabilities of the Agilent Oligo Pro II system and how it uses automated parallel capillary electrophoresis for purity analysis of oligonucleotides.

IC Systems can be tailored to meet specific anion and cation analysis needs providing direct determination of multiple analytes in a single and challenging sample matrices.

Learn key factors of method scaling and transfer. Understand the options and guidelines listed in the FDA guideline and USP <621>, <1224>. Tips and tricks.

The calculation of signal to noise ratio is a critical parameter during method development, method validation and routine monitoring the performance of a chromatographic method.

Learn how Uncle enables stability testing of biologics at high concentrations. Explore Tm, Tagg, and G22 measurements to assess conformational and colloidal stability in real development conditions.