Course Description:
This course introduces the concept of Loss on Drying (LOD) and its significance in pharmaceutical quality control. Participants will learn how LOD values can affect the quality of substances, including medicines, and how LOD differs from moisture content determination. The theory session covers best practices for performing LOD testing and selecting appropriate LOD dishes or bottles.
The hands-on session provides practical experience in conducting LOD tests on pharmaceutical materials in accordance with USP General Chapter <731> Loss on Drying, including proper technique and interpretation of results.
Pricing varies. Please inquire for more info at https://go.usp.org/Services.
Upon completion of this course, you will be able to
- Explain the concept of LOD and distinguish it from moisture content determination.
- Demonstrate the performance of LOD testing in pharmaceutical materials according to <731>.
Who should participate:
- National and private Pharmaceutical QC laboratories
- QA Manager
- QC Chemist
- QC Manager
- R&D