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