Labeling Requirements for Prescription Drugs, Updates, and Future Direction for Chapter 17 (Live Webcast)

Event

Medication misuse has resulted in more than 1 million adverse drug events per year in the United States. Patients’ best source (and often only source) of information regarding the medications they have been prescribed is on the prescription container label. Although other written information and oral counseling sometimes may be available, the prescription container label must fulfill the professional obligations of the prescriber and pharmacist. These obligations include giving the patient the most essential information needed to understand how to safely and appropriately use the medication and to adhere to the prescribed medication regimen.
This 90-minute webinar will cover the definition and purpose of USP Chapter <17> for prescription container labeling standards, an overview of the logic for this chapter, prescription labeling issues, and the relevant state regulations available. Furthermore, it explores the key concepts of USP General Chapter <17> on labeling along with the latest update for this chapter and future directions.

Who Should Participate:
Pharmacists
Practitioners
Pharmacy software vendors
State board of pharmacy personnel
Consumer advocate