Course Description:
This webinar will discuss USP General Chapters <724> and <1724> and will present the equipment, most common conditions, and challenges for the evaluation of the in vitro performance tests of drug products applied to the skin. Dosage forms that can be applied to the skin include ointments, pastes, creams, lotions, gels, foams, and transdermal systems. As some of these semisolid dosage forms can also be applied in the eye, a brief discussion on ophthalmic products will also be included.
Upon completion of this course, you will be able to:
- Know the definitions of the pharmaceutical dosage forms that can be applied to the skin
- Know the basic apparatus and most common conditions for the dissolution/drug release/in vitro release tests for these dosage forms
- Understand the purpose and application of the dissolution/drug release/in vitro release tests for drug products applied to the skin
- Be aware of the challenges presented by these tests for these dosage forms
Who Should Participate:
Scientists working with:
- Formulation and/or method development
- Stability studies
- Post-approval changes
- Regulatory affairs
- QA/QC Staff
The live version of this recording took place on March 28, 2024.
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
Dr. Margareth R. C. Marques
Principal Scientific Liaison, USP
Ph.D., Analytical Chemistry, State University of Campinas