We've updated our Privacy Policy to make it clearer how we use your personal data.

We use cookies to provide you with a better experience, read our Cookie Policy

Moving to Multi-Attribute Methodology (MAM) with a Compliant Single Solution

Webinar

 
Moving to Multi-Attribute Methodology (MAM) with a Compliant Single Solution
 
Sean McCarthy
Global Technical Marketing Manager, Biologics, SCIEX
 

In this webinar, you will learn how multiple attribute method (MAM) can accelerate your biotherapeutic development and quality control. The presented compliant solution takes advantage of leading MS quantitation software which offers flexibility in definition, integration, and calculation of targeted attributes.

We will discuss the aspects of defining attributes and calculation of their levels, setting acceptance criteria, and executing purity assessment using new peak detection. In addition, the presented workflow enables rapid and accurate data processing. Once defined, methods may be executed in a fully compliant environment to ensure data integrity and traceability with full audit trail support.

By attending you will learn how MAM enables you to:
- Accurately assess critical quality attributes using high resolution mass spectrometry
- Gain increased confidence in results using compliant workflows
- Collect and process comprehensive data with greater confidence to expedite your investigations
- Complete attribute assessments at the MS 1 level data while MS/MS data remains available as neededs

 
 
 
 

Like what you just read? You can find similar content on the communities below.

Analysis & Separations Biopharma Cell Science Drug Discovery Immunology & Microbiology

To personalize the content you see on Technology Networks homepage, Log In or Subscribe for Free

LOGIN SUBSCRIBE FOR FREE