Company officials were concerned about the length of time a…

Company officials were concerned about the length of time a particular drug product retained its potency. A random sample of 10 bottles of the product was drawn from the production line and analyzed for potency (fresh). A second sample of 10 bottles was obtained and stored in a regulated environment for a period of 1 year (stored). They test  H0: the true mean potency of the drug after 2 years is 10GM H1: the true mean potency of the drug after 2 years is different from 10GM Fill in the blanks by selecting from the dropdown menu. If the test determines that the true mean potency of the drug after 2 years is 10GM when it is actually different, then this is a [fill1] error.  If the test determines that the true mean potency of the drug after 2 years is different from 10GM when it actually is 10GM, then this is a [fill2] error. The [fill3] of the test is the probability that the test determines that the true mean potency of the drug after 2 years is different from 10GM when it is in fact different. The [fill4] of the test is the probability that the test incorrectly determines that the true mean potency of the drug after 2 years is different from 10GM.  

A ____ sterilised product undergoes a single sterilisation p…

A ____ sterilised product undergoes a single sterilisation process in a sealed container after preparation thus limiting the possibilities for error. quality sterile inventory cost terminally microorganisms lead time thermal chemical contamination advisory phase 2 chemical filtration external reconcile record-keeping system purchasing policy [BLANK-1]

Precautions to minimise ____ should be taken throughout the…

Precautions to minimise ____ should be taken throughout the preparation of aseptic products quality sterile inventory cost terminally microorganisms lead time thermal chemical contamination advisory phase 2 chemical filtration external reconcile record-keeping system purchasing policy [BLANK-1]

____ of dispensing includes the preparation and labelling of…

____ of dispensing includes the preparation and labelling of the prescribed medicine quality sterile inventory cost terminally microorganisms lead time thermal chemical contamination advisory phase 2 chemical filtration external reconcile record-keeping system purchasing policy [BLANK-1]