Course Description:This webinar series will update you on the latest USP developments in Particulate Matters.
This webinar will focus on USP General Chapter <771> and the applicability of USP’s visible (<790>) and subvisible (<788> and <789>) standards to ophthalmic drug products. Discussions will cover the evolution of USP chapters, methods and requirements, concepts of method qualification, and other technical considerations. Participants will be offered the opportunity to ask questions during the last segment of the session.
Who should participate:
- Laboratory scientists
- Lab managers
- QA/QC staff in the pharmaceutical and allied industries
- Regulatory professionals
- Scientists with interest in Particulate Matter