Quiz
RMSR Quiz 4 (Chapters 4 & 5)
Perguntas do quiz (16)
1Stem cells are responsible for creating all the different kinds of blood cells in the body and are usually found in bone marrow but can also circulate in the blood.
- AVerdadeiro
- BFalso
2Treated genes can be delivered into human cells only by means of a carrier, called a “vector”.
- AVerdadeiro
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3The “genome” is the template governing all the body’s cellular processes.
- AVerdadeiro
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4What has come of the Human Genome Project?
- AThe human genome is now almost fully sequenced.
- BAn individual’s genome can now be sequenced in less than an hour.
- COver 1,800 disease genes have been identified.
- DAll of these statements are correct.
5What is the process of manipulating genes to create medications and vaccines?
- Abionics
- Bgenetic engineering
- Concology
- Dspirometry
6What is the difference between gene therapy and recombinant therapy?
- AGene therapy enables the body’s own cells to produce the needed therapeutic proteins, whereas recombinant therapy relies on genetically modified microorganisms.
- BRecombinant therapy poses fewer potential risks to patients.
- CRecombinant therapy enables the body’s own cells to produce the needed therapeutic proteins, whereas gene therapy relies on genetically modified microorganisms.
- DNone of these
7Which of the following statements about gene splicing is INCORRECT?
- AGene splicing has been employed to produce vaccinations.
- BGene splicing is the process of inserting one organism’s genes into another to alter the types of proteins it produces.
- CGene splicing is used to farm insulin from E. coli.
- DGene splicing has been forbidden by the FDA.
8Monoclonal antibodies...
- A...are all derived from mice.
- B...are types of HAMAs.
- C...can be mass-produced.
- DMonoclonal antibodies are all of these things.
9The AMA is empowered to regulate medical devices to ensure their safety and effectiveness.
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10Though currently in the works, the FDA does not publish data on medical device recalls.
- AVerdadeiro
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11What is NOT accomplished by submitting a medical device to an effective reliability program?
- Asome confidence that inspection by regulatory bodies will not lead to major discrepancies
- Bregulatory measures against the misbranding or adulteration of medical devices
- Cregulation of medical devices during their design and development phases
- DEffective reliability programs accomplish all of these things.
12What was the FDA authorized to do after the Federal Food, Drug, and Cosmetic Act of 1938?
- Acontrol harmful radiation emissions from electronic products
- Bimplement the Preproduction Quality Assurance Program
- Cregulate medical devices during their design and development phases
- Dtake formal or informal regulatory measures against the misbranding or adulteration of medical devices
13What was an effect of the the U.S. Supreme Court’s ruling on Medtronic, Inc. vs. Lohr in 1996?
- AManufacturers have encountered increased pressure to produce safe, reliable devices.
- BManufacturers were granted immunity from civil liability suits regarding defective products.
- CThe federal government was granted permission to oversee medical devices' design and development phases.
- DThe FDA began classifying medical devices according to their level of risk to patients.
14What is NOT considered one of the important associated areas to consider when improving medical device reliability?
- Aaccuracy of measurements to assess risks
- Bamount it costs to maintain the device
- Camount of training required to maintain the device
- DAll of these associated areas are important.
15Although clinical studies are very valuable in the selling process, most healthcare professionals do not see them as credible sources of new information about medical products.
- AVerdadeiro
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16Over the life of an existing medical product, medical sales reps need to utilize medical evidence in order to persuade physicians to use an existing product for the treatment of a disease.
- AVerdadeiro
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Informações
- Descrição
- Medical Sales Quiz sobre RMSR Quiz 4 (Chapters 4 & 5), criado por silvertip83 em 20-12-2013.
- Autor
- silvertip83
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- English
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