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 ...
Need to improve throughput, lower detection limits, or other GC challenges? Join us to explore cutting-edge solutions for EPA ...
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 ...
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 ...
In this article, the author modestly expresses his views on the use and understanding of linearity, a key parameter to be determined in analytical method validation in quality control laboratories (QC ...
The primary impact of using the covalidation model is the expedited analytical method qualification of both the transferring and receiving laboratories. An important operation in the registration ...
Thermo Fisher Scientific Inc., has announced it has developed a faster screening method for pesticides, enabling labs to simultaneously screen and confirm the presence of more than 1000 pesticides, at ...
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