Learn about intriguing findings from work with USP Chapter <1469>, Procedure 1, and a successful implementation of Procedure 3.
Stay ahead and improve your skills! Receive tailored information on new separation science methods and applications.
Register for free learning now >>
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.
Find out why organizations cannot continue to advance with only technology and must also understand the evolution of data integrity.
In this forum the expert panel will discuss technologies and strategies for streamlining biopharmaceuticals production.
Stay ahead and improve your skills!
Be the first to know as our team will send straight to your inbox tailored information on new separation science methods and applications..