Allowed Adjustments to Pharmacopeia HPLC Methods

This webinar will provide a detailed understanding of new revisions to allowed adjustments for USP and Ph. Eur. HPLC methods through the use of case studies.

• Intro: Review revisions to allowed adjustments for USP and Ph. Eur.
• Isocratic Case Study: Adjustments to column length and ID, particle size, and flow rate
• Gradient Case Study: Adjustments to column length and ID, particle size, flow rate, and gradient timetable

Key Learning Points:

• Review of recent revision to allowed adjustments for USP and Ph. Eur. HPLC methods
• Utilize a case study to highlight the approach for making adjustments to an isocratic method and the resulting benefits
• Understand the benefits of working within the allowed adjustments for improving the performance of compendial HPLC methods (isocratic and gradient) in your laboratory

Who Should Attend:

Scientists and analysts in the pharmaceutical industry who work with Pharmacopeia HPLC methods that are interested in:

• Improving performance
• Reducing analysis time
• Understanding allowable adjustment application examples

Presenter: Phil Koerner (Global Pharmaceutical Market Development Manager, Phenomenex)