PEBC questions with verified answers
7 regulations Part A-J Ans✓✓✓ Part A- Administration - contains information on
prohibition, powers, definitions and obligations
Part B - Food - contains information on general labeling, nutrition, labeling,
standards of compositions, food additives and food packaging materials
Part C - Drugs - used to contain schedule F drugs which are now replaced with the
prescription drug list. It is a list of medicinal ingredients that, if found in a drug,
requires a prescription for sale in canada. PDL does not include drugs that are
regulated under CDSA (narcs). There are two separate PDLs for human and
veterinary use.
Part D - vitamins minerals and amino acids - contains foods that must or can be
fortified with vitamins and minerals.
Part E - cyclamate and saccharin sweeteners - regulates the labeling and
advertising of cyclamate and saccharin artificial sweeteners.
Part G - controlled drugs - contains information regarding the possession, sale,
production and transportation of controlled drugs ( controlled drugs are regulated
under CDSA)
Part J - Restricted drugs - contains information regarding the possession,
production, sale and transportation, and inspiration of restricted drugs for clinical
trials or research purposes
Absorption bases Ans✓✓✓ water absorbing properties. Two types of bases are
anhydrous,and water without emulsions. Readily permit incorporation of water,
will absorb water and contain water. EX: hydrophilic petrolatum-contains
cholesterol, stearyl alcohol, white wax, white petrolatum. Aquaphor is a
commercially prepared base
accessibility Ans✓✓✓ Canadians must have reasonable access to insured services
without charge or paying deductibles or copays
, area under the curve Ans✓✓✓ integral of plasma concentration over the interval
of time
Automony Ans✓✓✓ respecting the patient's choice or free will, choose or refuse
treatment or action such as dispensing
Average BSA Ans✓✓✓ 1.73 m^2
Beneficence Ans✓✓✓ doing good or promoting the patient's best interest in the
decision taken
bioavailability Ans✓✓✓ percentage of administered drug that arrives in the
central compartment
blending Ans✓✓✓ process of mixing powders to be incorporated into the final
drug product
Canada Vigilance program Ans✓✓✓ post-market surveillance program that
collects and assesses reports of suspected adverse reactions to health products
marketed in Canada.
Comminution Ans✓✓✓ reducing the size of particles or aggregates through
cutting, chopping, crushing, grinding, milling, micronizing and triturating
comprehensiveness Ans✓✓✓ provincial health insurance programs must include
all medically necessary services. The Canada health act defines
7 regulations Part A-J Ans✓✓✓ Part A- Administration - contains information on
prohibition, powers, definitions and obligations
Part B - Food - contains information on general labeling, nutrition, labeling,
standards of compositions, food additives and food packaging materials
Part C - Drugs - used to contain schedule F drugs which are now replaced with the
prescription drug list. It is a list of medicinal ingredients that, if found in a drug,
requires a prescription for sale in canada. PDL does not include drugs that are
regulated under CDSA (narcs). There are two separate PDLs for human and
veterinary use.
Part D - vitamins minerals and amino acids - contains foods that must or can be
fortified with vitamins and minerals.
Part E - cyclamate and saccharin sweeteners - regulates the labeling and
advertising of cyclamate and saccharin artificial sweeteners.
Part G - controlled drugs - contains information regarding the possession, sale,
production and transportation of controlled drugs ( controlled drugs are regulated
under CDSA)
Part J - Restricted drugs - contains information regarding the possession,
production, sale and transportation, and inspiration of restricted drugs for clinical
trials or research purposes
Absorption bases Ans✓✓✓ water absorbing properties. Two types of bases are
anhydrous,and water without emulsions. Readily permit incorporation of water,
will absorb water and contain water. EX: hydrophilic petrolatum-contains
cholesterol, stearyl alcohol, white wax, white petrolatum. Aquaphor is a
commercially prepared base
accessibility Ans✓✓✓ Canadians must have reasonable access to insured services
without charge or paying deductibles or copays
, area under the curve Ans✓✓✓ integral of plasma concentration over the interval
of time
Automony Ans✓✓✓ respecting the patient's choice or free will, choose or refuse
treatment or action such as dispensing
Average BSA Ans✓✓✓ 1.73 m^2
Beneficence Ans✓✓✓ doing good or promoting the patient's best interest in the
decision taken
bioavailability Ans✓✓✓ percentage of administered drug that arrives in the
central compartment
blending Ans✓✓✓ process of mixing powders to be incorporated into the final
drug product
Canada Vigilance program Ans✓✓✓ post-market surveillance program that
collects and assesses reports of suspected adverse reactions to health products
marketed in Canada.
Comminution Ans✓✓✓ reducing the size of particles or aggregates through
cutting, chopping, crushing, grinding, milling, micronizing and triturating
comprehensiveness Ans✓✓✓ provincial health insurance programs must include
all medically necessary services. The Canada health act defines
