Download this eBook, produced in collaboration with Agilent, to discover the latest regulations, tools, and techniques in pharmaceutical impurity analysis.
Examine the regulatory crossroads resulting from the ubiquitous presence of PFAS in widely prescribed drugs.
Learn about intriguing findings from work with USP Chapter <1469>, Procedure 1, and a successful implementation of Procedure 3.
Discover a sensitive quantitative LC-MS/MS method developed for the simultaneous analysis of eleven highly polar nucleotide sugars
Practical strategies to decrease uncertainty in comprehensive extractables and leachables analysis by LC/MS
Learn practical strategies to decrease uncertainty in comprehensive extractables and leachables analysis by LC/MS.
Find out about acceptance from regulators on new technology and other key issues regarding Pharma 4.0.
Find out about changes to the pharmaceutical manufacturing processes during and post the COVID pandemic
The role of dissolution as a quality assurance tool for product development, approval and batch release, the use of dissolution testing of novel drug formulations and how...
This forum will focus on data integrity and compliance, particularly in the context of QA/QC, development, and manufacturing.
Applying an enhanced approach to the lifecycle of analytical procedures from development through validation will be discussed.
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