In order to meet US EPA or FDA requirements, a method must meet many stringent requirements. Areas Covered in this Webinar: The more important of these for specific analytical methods are method ...

A newly developed software program transforms written SOPs for all required analytical method validation experiments into transferable automated templates, integrating individual activities and ...

In collaboration with scientists from the European Union Reference Laboratory for Dioxins and PCBs in Feed and Food, Thermo Fisher Scientific has developed a simple, reliable and robust method for ...

Dublin, Feb. 27, 2025 (GLOBE NEWSWIRE) -- The "3hr Virtual Seminar - Validation, Verification and Transfer of Analytical Methods - Implementing Guidelines from FDA/EMA, USP and ICH" training has been ...

Thermo Fisher Scientific has announced a new gas chromatography (GC) method for the analysis and quantifying of residual solvents in pharmaceutical products and excipients as a result of the ...

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 ...