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) 3 B) 1 C) 10 D) none needed
A) false B) true
A) verify validity with external laboratory testing B) every 6 months immediately after washing, garbing, and gloving C) immediately after media-fill test 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) ensure personnel being tested do NOT disinfect gloves before the test C) no need to worry about positive and negative control since they cancel each other out
A) false B) true
A) opened growth media plate B) both opened and/or unopened C) disinfected vial D) unopened growth media plate
A) all options are correct B) during hand washing, garbing, and gloving C) right before hand washing, garbing, and gloving D) immediately following hand washing, garbing, and gloving |