Analytical methods must be validated to provide reliable data for regulatory submissions. These methods are essential for a number of purposes, including testing for QC release, testing of stability ...
Method development scientists looking to maximize efficiency and further improve pH stability and column reliability for reverse phase chromatography should look no further, according to Waters ...
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 ...
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 ...
High performance liquid chromatography (HPLC) has become an essential technique in pharmaceutical analysis for the separation, identification, and quantification of pharmaceuticals. Due to its high ...
A one-of-a-kind, user-friendly software, LabSolutions MD integrates method scouting, data acquisition, and data processing, and uses analytical quality by design (AQbD) principles, to save users time ...
Learn how to navigate the regulatory landscape utilizing current method development technologies for impurity control in late-phase API manufacturing. This webinar will cover the method development ...
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