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Chapter Review Pharm
Chapter Review Pharmacy Quality Assurance
| P&T (Pharmacy and Therapeutics) develops: | The formulary for an institution. |
| Substances that require Safety Data Sheets are: | Investigational drugs. |
| Date of repackaging: | Is not required on on the label of a repackaged medication. |
| An employee that is exposed to pathogens should submit a report to: | The CDC . |
| Hypoallergenic gloves should be changed: | Hourly. |
| The federal responsible for oversight of the SDS sheets is: | OSHA. |
| The organization that oversees the Medwatch is: | The FDA. |
| The document that is used to document medication administered to a patient: | MAR |
| The HEPA filter must be certified : | Every 6 months |
| Pharmacy weights must be recalibrated: | Once a year. |
| GMP stands for: | Good manufacturing practices. |
| The organization that establishes non sterile and sterile compounding requirements: | United States Pharmacopeia |
| ISMP has two error-reporting programs: | ISMP-MERP (medication) and ISMP-VERP (vaccination). |
| Countertops and counting trays are cleaned using: | 70% isopropyl alcohol. |
| Laminar flow hood should be cleaned: | Using 70% isopropyl alcohol. |