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A monthly buying budget is created based on the pharmacy's planned
sales
How must pharmacies store Schedule II controlled substances?
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In a safe or locked cabinet.
DEA's Controlled Substance Ordering System (CSOS)
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allows for secure electronic transmission of Schedule I-V controlled
substance orders without the supporting paper Form 222 and can be
accessed at the DEA’s E-Commerce Program website (www.DEAecom.gov).
What is one purpose of State Boards of Pharmacy?
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Licensing or registration of pharmacists, technicians, and other pharmacy
personnel.
How do health care facilities obtain an EPA identification number?
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By submitting a site identification form to the appropriate EPA regional
administrator
Third Party Logistics Provider (3PL)
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Also known as a "3PL", these entities possess products but do not own
them. They act as a warehouse, receiving products sent to them by a
manufacturer, and distributing orders as directed by the manufacturer.
,How long must health care facilities keep a copy of the signed shipping document?
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Health care facilities must keep a copy for 3 years.
What application must drug developers submit to the FDA before starting clinical
research?
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Investigational New Drug (IND) application.
What does the Protecting Our Pharmaceutical Supply Chain From China Act of
2020 aim to track?
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Active pharmaceutical ingredients through an FDA registry.
What must a health care facility provide to the EPA if it does not receive the signed
shipping document?
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, A copy of the manifest along with an explanation of efforts taken to locate
the hazardous waste and the results of those efforts.
Scheduling an order for ten days before a patient’s next refill is an example of:
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Just in time ordering
503A Compounding
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A pharmacy may compound prescription products, but only for a specific
patient on a prescription or order from a provider. Pharmacies may NOT
compound any commercially available product unless there is a significant
clinical reason to do so. Some examples include compounding a liquid
medication for an infant when the commercially available medication is
only available as a tablet and compounding a medication without dye when
a patient is allergic to the dye in the available product.
If a commercial product is not available in the marketplace (there is an
FDA-documented shortage), then a pharmacy may compound that product
for the specific patient but only during the time the product is in shortage.
What is included on the IND application?
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