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 ...
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 ...
Concept of damage-free dry transfer printing using stress engineering. a, b) Schematic illustrations describing the formation of a single (a) and bilayer (b) structured Pt thin films. c) Stress ...
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