What are the possible lab hazards that may occur during the processing and manufacturing of drugs in industry?

If a hazardous drug on the REMs list is prescribed for a patient- the following is required to be done in order to dispense the drug, except: A) need to be enrolled in the REMs program B) patient must show they can afford the drug C) patient and physician agreement form needs to be completed D) patient will be counseled on the risks of the drug

A(n) -------------------phase is almost always needed so that refinements to the intervention can be made and its acceptability can be assessed.

The Food and Drug Administration (FDA) is responsible for: A. Requiring drug manufacturers to provide notice that a new drug is safe. B. Recalling pharmaceuticals only after harm has occurred. C. The approval before a new drug can be marketed. D. The assumption that the manufacturer of drugs would have conducted safety tests before marketing a new drug and protocols have been established.

Outline the general steps from initial drug discovery to IND filing. Add as much detail as you need and feel free to use flow charts, graphics, visuals, as long as is made by you alone and not directly copied-pasted from another source. If an IND is cleared to proceed by the US-FDA, what is the single most important goal of a first-in-human (FIH) clinical trial?

What is the advantages and disadvantages of productive management in the laboratory environment? (Please give some examples)

According to the standard of practice VIII, how should loaner instrumentation be processed in SPD? How do we protect the facility (hospital)?

How can you identify a controlled substance just by looking at the label of a medication?

Strict Liability can be simply defined as:   A)  plaintiff liability.   B)  liability without fault.   C)  dram shop laws.   D)  extreme negligence.

Create a list of ten drugs and include each of the following: Chemical name Generic name Official name Trade or brand name