Raman and SEM-EDS in pharmaceutical quality control, failure analysis and compliance


Originally Aired December 1, 2021
 

Your details

Our registration process uses cookies. By submitting this registration form you agree to our cookie policy.

(*) denotes required form field(s)

  Register

Raman and SEM-EDS in pharmaceutical quality control, failure analysis and compliance


Originally Aired December 1, 2021
 

Overview

If you’ve already registered, please click here to log in to the webcast.

Analytical tasks in the pharmaceutical industry range from drug discovery to production and quality control for consumer product. This entire process is subject to a variety of laws and regulations and requires careful examination at every step.

This webcast aims to show how Raman microscopy and SEM-EDS, as complementary measuring techniques, can contribute at every stage of pharmaceutical development to identify and characterise materials of interest.

Raman spectroscopy is a well-established non-destructive analytical method for identifying the unique chemical composition of sample components. In addition to the standard chemical identification and distribution analysis delivered by SEM-EDS, users can now take advantage of Live Chemical Imaging capability afforded by current large area EDS detectors.

Furthermore, Raman imaging can be integrated within the vacuum chamber of scanning electron microscopes, combining the highest-resolution structural characterisation with the capability of elemental analysis through EDS. This correlative approach is used to identify and characterise at every stage of pharmaceutical production, including:

  • Raw ingredients (Quality Control)
  • End product (Quality Control, Failure Analysis and Counterfeit ID)
  • Packaging (Quality Control, Failure Analysis and Counterfeit ID)

In addition to obtaining reliable results, both techniques are increasingly being incorporated into SOPs within regulated environments.

Learn:

  • Insights into the role of Raman and SEM-EDS analysis in the pharmaceutical industry
  • How to analyse drug delivery systems
  • How pharmaceutical packaging can be analysed for defects and counterfeit identification

This webcast has been produced by Oxford Instruments, who retains sole responsibility for content. About this content.

Presenters

Presenter
Anthony Hyde
Product Manager
Oxford Instruments
View Biography
Presenter
Dr. Ute Schmidt
Applications Manager
WITec
View Biography
Presenter
Moderator: Sarah Hiddleston
Science Journalist
Nature Research Custom Media
View Biography