Webinar: Changes to USP <1788> Subvisible Particulate Matter

May 27, 2021


Participate in a complimentary webinar as we uncover the new version of the USP chapter on Subvisible Particulate Matter, USP <1788>, which became official on May 1st.  Users are encouraged to develop a particle sizing and counting strategy using an integrated approach of orthogonal, complementary scientific methods in order to forensically characterize and possibly identify the particle population in injectable dosage form drug products.

Register today

Tony Harrison, Senior Marketing Manager, will cover the changes and the new recommendations. At the end of the webinar, you will:

  • Know more about a holistic approach to particle sizing and characterization recommended by the new USP<1788> chapter, from drug discovery, through process development and on to final product quality control in the GMP manufacturing environment.
  • Understand the difference between the compendial HIAC pass/fail test and complementary orthogonal testing methods for particle characterization.
  • Understand why HIAC was chosen in the first instance to supersede the traditional microscopy method, and why it remains the preferred instrument for compendial pass/fail Limit testing.

Register today