Course Description:This course will provide information on USP Reference Standards as highly characterized chemical specimens required for use in USP–NF compendial methods. The course offers a detailed look at types of Reference Standards and practical application. Information related to the science behind Reference Standard development as well as specific cases, and USP support services will also be covered.
Upon completion of this course, you will be able to:
- Describe the importance of the Reference Standard Development Process
- Determine why USP RS—Regulatory Directives are used
- Describe the proper use of USP Reference Standards
Who Should Participate:
- Laboratory scientists
- Laboratory managers
- QA/QC staff in the pharmaceutical and allied industries
- Regulatory professionals
The live version of this recording took place on July 17, 2024.
There will be a knowledge assessment at the end of the course. If this course is taken as part of the USP certificate program, you will be required to pass this knowledge assessment with a score of 80 percent to determine if your comprehension of the topics presented meets USP’s minimum requirements.
Access Duration:
Access to this course expires 60 days from the date of registration or until you mark the course ‘Complete’ – whichever occurs first.
USP Approved Instructor
Robert Shimihara
USP Staff
RPO Strategic Projects Director - RPO Chemical Medicines
B.S., Chemistry, University of Redlands, California