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USP 788 Requirements and Solutions

Release of parental drugs for injection requires test apparatus to be accurate, precise, reliable and compliant with the latest international regulation. Learning how to keep a Light Obscuration particle counter under continuous control, guarantying steady performance, is the key to commercialize quality products and ensure patient safety. This webinar will cover the key international requirements to properly perform particle count testing in injectable liquid, including instruction and best practices to run meaningful and frequent suitability test.

Key Learning Objectives:

  • USP 788 Solution for monitoring your liquids.
  • International requirements for particle count testing in injectable liquids.
  • Instructions and best practices on how to run meaningful and frequent suitability tests.

Who Should Attend:

  • QA/QC/Microbiology
  • Operations Management
  • Engineers
  • System Owners

Watch the Webinar now

  • Presenter

    Daniele Pandolfi

    Global Product Line Manager, Aerosol, Particle Measuring Systems

    Daniele Pandolfi is the Global Product Line Manager, Aerosol in Particle Measuring Systems’ Life Science Division. He has over eleven years’ experience in particle counter instrumentation and cleanroom contamination control, focusing on strong customer relationships. He has helped many cleanroom users solve their cGMP issues. Mr. Pandolfi has been responsible for the EMEA Service Department, and a member of the Global Life Science organization in 2015.

  • Presenter

    Heather Mason

    Microbial Product Sales Specialist, Particle Measuring Systems

    Heather Mason is a Microbial Specialist working with the America’s Sales Managers at Particle Measuring Systems, providing insight and customer assistance with microbial monitoring process and products. Before joining PMS, Heather worked over 10 years as a pharmaceutical Quality Control Manager for a vaccine company and as Quality Manager for a solid oral dose pharmaceutical manufacturing company.