When:  Tues, April 20, 2021

Key learning objectives:

• Learn how to navigate challenges encountered when meeting Data Integrity guidelines
• Understand compliance risks associated with electronic and paper data (ALCOA+)
• Hear how the right choice of FTIR instrument can enable data integrity
• Learn about the evolution of Mass Spectrometry in Pharma QC
• Understand importance of selecting the right CDS to ensure data integrity and compliance for MS

Who should attend:

• Analytical science and technology transfer leaders
• Analytical scientists working in biopharmaceutical manufacturing
• QC managers

REGISTER HERE