Nitrosamine Testing using LC-MS Methods from the USP General Chapter
Learn about intriguing findings from work with USP Chapter <1469>, Procedure 1, and a successful implementation of Procedure 3.
Pharmaceutical Manufacturing
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Analysis of Nucleotide Activated Sugars by LC-MS/MS
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.
Regulatory Challenges in Pharma 4.0
Find out about acceptance from regulators on new technology and other key issues regarding Pharma 4.0.
Impact of COVID on Pharma 4.0
Find out about changes to the pharmaceutical manufacturing processes during and post the COVID pandemic
Dissolution: Today, Tomorrow & Beyond
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...
Facilitating Data Integrity & Compliance
This forum will focus on data integrity and compliance, particularly in the context of QA/QC, development, and manufacturing.
Pharma 4.0: Analytical Procedure Lifecycle Management
Applying an enhanced approach to the lifecycle of analytical procedures from development through validation will be discussed.
The Importance of Data Integrity in Achieving Pharma 4.0
Find out why organizations cannot continue to advance with only technology and must also understand the evolution of data integrity.
Pharma 4.0 – 2021: Streamlining Biologics Production
In this forum the expert panel will discuss technologies and strategies for streamlining biopharmaceuticals production.
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