News Articles Tagged: Method Development

Ensuring Drug Efficacy: The Critical Role of Pharmaceutical Reference Standards and Analytical Method Development

Learn why pharmaceutical reference standards and robust analytical method development are vital for ensuring the quality, safety, and efficacy of drugs like Rivaroxaban.

Practical Guide: Using Sodium 1-Heptanesulfonate for Effective HPLC Method Development

A practical guide on how to effectively use Sodium 1-Heptanesulfonate in HPLC method development to achieve optimal separation of ionic compounds and enhance analytical outcomes.

From Lab to Market: Navigating the Validation of Analytical Methods for Rivaroxaban Impurities

NINGBO INNO PHARMCHEM CO.,LTD. discusses the critical process of validating analytical methods for Rivaroxaban impurities, ensuring accuracy and reliability.

Mastering Rivaroxaban Impurity Detection: A Guide to Analytical Challenges

Explore the analytical challenges in detecting Rivaroxaban impurities and how NINGBO INNO PHARMCHEM CO.,LTD. addresses them with advanced techniques.

Optimizing HPLC Separations: The Strategic Use of Silane Monomers

Learn how strategic selection and use of silane monomers like N-Butyldimethylchlorosilane are key to optimizing HPLC separations, achieving greater precision and efficiency in analytical workflows.

Navigating Cefuroxime Purity: The Role of Cefuroxime EP Impurity I in Analytical Method Development

Discover how Cefuroxime EP Impurity I (CAS 39684-61-2) facilitates accurate analytical method development for Cefuroxime, a key step in drug efficacy.