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