Course Description:An informative webinar on the latest updates to USP Chapter <697> Container Content for Injections, which outlines important guidelines for ensuring accurate withdrawal of labeled drug quantities from injection containers. The webinar will highlight the harmonization of this chapter with the European and Japanese Pharmacopeias, as well as address specific national USP requirements. We will cover key updates on procedures for measuring injection volumes in single-dose, multi-dose, and large-volume intravenous solutions, including handling suspensions, emulsions, and oily preparations to ensure precision. Attendees will gain valuable insights into the revised standards and learn how to maintain compliance with both harmonized and national text, crucial for ensuring product quality.
Who Should Participate:
- Chemistry Manufacturing Control, including Drug Product Processing (Analytical, Formulation, Fill/Finish) and Device
- QA/QC staff in the pharmaceutical and allied industries
- Regulatory professionals