USP <797> and USP <800>

3. CSP microbial risk categories reduced to ___
4. date or time after which a CSP cannot be used and must be discarded
7. type of sterilization that includes dry heat or steam
8. personnel who have not compounded CSPs in more than 3 ___ must be requalified in all core competencies before resuming compounding duties
10. this type of sampling evaluates hand hygiene and garbing
11. in-___ time refers to the time before which a conventionally manufactured product used to make a CSP must be used after it has been opened or punctured
16. airflow moving in a single direction in a uniform manner
17. extent to which a CSP retains physical and chemical properties throughout its BUD
19. type of air exiting the HEPA filter in a unidirectional air stream
20. must be removed before entering a compounding area

1. each CSP must be sterile and ___-free before release
2. avoid this type of sterilization if moisture would degrade the CSP
5. chemical agent used on inanimate surfaces and objects to destroy fungi, viruses, and bacteria
6. free from viable microorganisms
8. designed to contain more than one dose of the medication
9. <800> covers the handling of ___ drugs
12. process of adding a diluent to a powdered medication to prepare a sterile solution or suspension
13. <797> describes requirements and standards of ___ products
14. this area must provide at least ISO Class 7 air quality
15. substance added to inhibit microbial growth
18. sterile compounding requires ___ manipulation