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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 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 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 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]

A customer complaint

Makoma is a boy

Sterilisation by filtration of bulk fluids is the method of choice in aseptic manufacturing of a sterile medicinal product when the final sterilisation in the container closure system is not possible/suitable

Aseptic technique is a set of specific practices and procedures performed under carefully controlled conditions with the goal to minimise contamination by microorganisms and maximise asepsis.

You have to prepare 50 g of Zinc and Ichthammol Ointment. The recipe for the ointment is Zinc Oxide 10 gIchthammol 9 gWool fat 9 gSoft yellow paraffin 72 gCalculate the quantities needed to prepare 50 g of the ointment 

Fill in the missing terms from the list  ———————–is the sum of all the items you carry as stock. 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]