Ensuring reliable analytical methods and bioassays requires a well-thought-out strategy for evaluating method validity and systems suitability. Analytical methods and bioassays require a ...

Analytical Methods welcomes developments in, and early applications of, innovative analytical methods and techniques that demonstrate real-world potential for societal impact across disciplines. We ...

Techniques like SPME and QueChERS enhance sustainability by minimizing solvent and consumable use in sample preparation. With ...

In today’s pharmaceutical environment, where compliance and speed-to-market are paramount, analytical method development and validation play a foundational role. From early research through to GMP ...

The article proposes an integration of method validation, transfer, and verification process into the overall lifecycle management process. The US Pharmacopeial Convention (USP) released a general ...

The attributes of the DS or DP that are to be tested to obtain the necessary information about product quality safety and efficacy are determined during the Drug Development stage. The information ...

Regulatory expectations and requirements continue to evolve to ensure the quality and safety of drug products. Over the last five years, we have seen increased focus during regulatory inspections ...

In the pharmaceutical industries, validation of analytical methods is a critical process that confirms the reliability and appropriateness of a method for its intended application. Method validation ...

DUBLIN--(BUSINESS WIRE)--The "Analytical Method Validation, Verification and Transfer Virtual Seminar (Oct 7th - Oct 9th, 2025)" has been added to ResearchAndMarkets.com's offering. Dependable ...