DUBLIN--(BUSINESS WIRE)--The "Validation, Verification and Transfer of Analytical Methods (Understanding and implementing guidelines from FDA/EMA, USP and ICH)" conference has been added to ...

DUBLIN--(BUSINESS WIRE)--The "Validation, Verification and Transfer of Analytical Methods (Understanding and implementing guidelines from FDA/EMA, USP and ICH)" conference has been added to Research ...

In pharmaceutical organizations, developing and validating chromatographic methods is a routine, yet resource-intensive, task. Once a method is optimized and performs reliably, it’s natural to expect ...

The best way to ensure consistency as bioassays are transferred among labs and scaled up is to plan early on for those transfers. “Don’t back yourself into a corner,” Andrew Taylor, DPhil, associate ...

As analytical technology continues to advance, both regulatory agencies and pharmaceutical companies are keen to avail themselves of these enhancements. In the case of chromatography, evolution from ...