Course Description:
This course provides participants with foundational conceptual knowledge of Uniformity of Dosage Units (UDU), including its purpose in pharmaceutical quality control and its impact on product consistency. The theory session covers procedures for performing UDU testing using either weight variation or content uniformity, along with the formulas used for calculation, interpretation of acceptance values, and examples from relevant monographs. Best practices for conducting UDU testing are also discussed.
The hands-on session offers participants the opportunity to perform UDU analysis and calculate results in accordance with USP General Chapter <905> Uniformity of Dosage Units.
Pricing varies. Please inquire for more info at https://go.usp.org/Services.
Upon completion of this course, you will be able to
- Demonstrate understanding of the basic concepts of UDU, including procedures, calculations, and interpretation of acceptance values
- Perform UDU analysis and calculate results in compliance with <905>
Who should participate:
- National and private Pharmaceutical QC laboratories
- QA Manager
- QC Chemist
- QC Manager
- R&D