This webinar series will keep you informed of the latest USP developments on Particulate Matters.
For this introductory session, we will provide an overview of current USP standards on particulate matter and compare and contrast to what is published in the European and Japanese Pharmacopoeia.
Subject area:
Drug Products & APIs
Objectives (If applicable):
n/a
Target Audience (If applicable):
– Laboratory scientists
– Lab managers
– QA/QC staff in the pharmaceutical and allied industries
– Regulatory professionals
– Scientists with interest in Particulate Matter