Course Description:
This course introduces the concept of Residue on Ignition (ROI) and its relevance in pharmaceutical testing, particularly in identifying and quantifying inorganic impurities. Participants will learn how ROI values relate to the purity and quality of substances, including medicines. The theory session covers best practices for performing ROI testing, including proper technique and calculation methods.
The hands-on session provides practical experience in conducting ROI analysis in accordance with USP General Chapter <281> Residue on Ignition, ensuring participants are equipped to perform and interpret results accurately.
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 ROI and its role in pharmaceutical quality control
- Demonstrate ROI testing performance in pharmaceutical materials according to USP General Chapter <281>
Who should participate:
- National and private Pharmaceutical QC laboratories
- QA Manager
- QC Chemist
- QC Manager
- R&D