A new Tel Aviv University-led study published on May 20 in Nature offers new evidence that the complexity of contemporary analytical methods in science contributes to the variability of research ...

A new study offers new evidence that the complexity of contemporary analytical methods in science contributes to the variability of research outcomes. A new Tel Aviv University-led study published on ...

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 quality-by-design principles used to control process variability are equally important to measurement systems because process variability includes contributions from measurement system variability ...

Bioanalytical method development and validation are at the forefront of ensuring rigorous, reproducible and reliable data in both drug development and clinical diagnostics. The field encompasses the ...

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 ...

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 ...