• Discuss how to explain to licensees the ways in which proper facility design facilitates the maintenance of a state of control.
• Differentiate between ISO 5, 7, and 8 area cleanliness and particulate counts.
• Describe the function of HEPA filters in cleanroom environments and the application of airflow principles to create a sterile compounding environment.
• Compare sterile facility requirements outlined in USP 797 with those expected in a CGMP environment.
• Differentiate the engineering controls used in the preparation of nonhazardous versus hazardous compounded sterile preparations.
• Identify and differentiate between the various tests performed during certification of primary and secondary engineering controls.
• List the types of laminar airflow systems (LAFS) that may be utilized.
- Provider:TRC Healthcare
- Activity Link: https://www.criticalpoint.info/activities
- Start Date: 2022-07-18 05:00:00
- End Date: 2022-07-18 05:00:00
- Credit Details: Pharmacy: 2.5 hours
- Commercial Support: No
- Activity Type: Live Course
- CME Finder Type: Conference
- Fee to Participate: Yes
- Measured Outcome: Learner Knowledge
- Provider Ship: Directly Provided
- Registration: Open to all