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