Unit 1: State of Control: Environmental Practices for Sterile Compounding
Participants will gain a comprehensive understanding of environmental control requirements within the cleanroom suite and learn how to select the proper materials and cleaning agents to maintain a controlled environment. The course will also address best practices for investigating and remediating environmental excursions, ensuring that issues are resolved effectively and sustainably. Through structured guidance and practical application, learners will strengthen their ability to oversee competency processes with confidence. By the conclusion of the session, attendees will be prepared to uphold the rigorous standards essential to safe, compliant, and high-quality sterile compounding.
Learning Objectives:
- Describe the specific environmental control requirements in the cleanroom suite.
- Select appropriate materials and cleaning agents for use in the cleanroom suite.
- Demonstrate correct hand hygiene, garbing, and material/personnel movement techniques to minimize contamination risk.
- Investigate environmental monitoring excursions, determine root causes, and implement/document effective corrective and preventative actions.
Devonne Moore
Director of Clinical Quality
KabaFusion
Devonne Moore is the Director of Clinical Quality at KabaFusion. She earned her PharmD from Massachusetts College of Pharmacy and Health Sciences in 2014 after working in compounding pharmacy since 2009. Devonne has worked in both 503A and 503B facilities focusing on formulations. In her current role she works with team members across the country on cleanroom operations as well as inspection preparation and remediation.
NHIA Requires planners, faculty, and others who affect the content of this activity to disclose all financial relationships they have with ineligible companies. All relevant financial relationships are thoroughly vetted and mitigated according to policy.
Devonne Moore has no relevant financial relationships with ineligible companies to disclose.