Overcoming the Challenges of Nitrosamine Analysis Using LC-MS/MS
Discover how LC-MS/MS can help tackle key challenges in nitrosamine analysis.
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Discover how LC-MS/MS can help tackle key challenges in nitrosamine analysis.
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Explore the lessons learned from environmental PFAS applications and how these insights can be transitioned to other arenas.
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.
On-Demand
Karl Fischer Titration is the preferred technique in various industries, including pharmaceuticals. Our speakers will guide you to meet regulatory compliance.
On-Demand
Learn about the principles and importance of U/HPLC method adaptation in pharmaceutical analysis and how to boost laboratory effectiveness and efficiency.
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
Applying an enhanced approach to the lifecycle of analytical procedures from development through validation will be discussed.
In this forum the expert panel will discuss technologies and strategies for streamlining biopharmaceuticals production.
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