A) to eliminate contamination accumulated under the fingernails B) it allows your fingertip to become more susceptible to non-hazardous products C) because it is almost impossible to compound without fingertips D) assesses ability of personnel to maintain sterility of hands and fingertips during handwashing, garbing, and gloving as well as during sterile compounding
A) 3 B) 10 C) none needed D) 1
A) true B) false
A) immediately after media-fill test B) verify validity with external laboratory testing C) every 6 months immediately after washing, garbing, and gloving D) all the options are correct E) three consecutive successful times times prior to authorizing personnel
A) all options are correct B) label, seal, package, and ship samples, provide all required information, and ship samples as per third party instructions C) ensure external entity providing services has satisfied vendor qualification procedures D) review results and ensure CFU counts are within standards
A) true B) false
A) all tests can be groupped B) no need to worry about positive and negative control since they cancel each other out C) ensure personnel being tested do NOT disinfect gloves before the test
A) false B) true
A) both opened and/or unopened B) unopened growth media plate C) opened growth media plate D) disinfected vial
A) during hand washing, garbing, and gloving B) immediately following hand washing, garbing, and gloving C) right before hand washing, garbing, and gloving D) all options are correct |