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  • Question 1 and answer for basic drug training. PDF

       2026-02-25 NetworkingName910
    Key Point:Question 1 and answer for basic drug training - page 1Question of a drug basics testName: score:I. Filling out of the question. (1 minute per space, 30 minutes)1. Drugs are the type of disease used, diagnosed and designed to regulate the human bodySubstances that can or may not be specified,, in quantities including chinese medicine, chinese medicineDrinking tablets, chinese medicines, chemicals and their preparations, antibiotics, biochemicals,

    Question 1 and answer for basic drug training - page 1

    Question of a drug basics test

    Name: score:

    I. Filling out of the question. (1 minute per space, 30 minutes)

    1. Drugs are the type of disease used, diagnosed and designed to regulate the human body

    Substances that can or may not be specified, , in quantities including chinese medicine, chinese medicine

    Drinking tablets, chinese medicines, chemicals and their preparations, antibiotics, biochemicals, radiopharmaceuticals, serums, vaccines, blood production

    Products, diagnostic drugs, etc.

    2. The national food and drug regulatory authority has almost completed the year with the harmonization of approval symbols. Drugs approval symbol

    The uniform format is:。

    3. Prescription medicines are those that must be supplied and used only by and at the prescription level。

    Non-prescribed drugs (bbs): medicines that do not require prescription by a medical practitioner, and those used.

    5. The special marking pattern for non-prescription drugs is divided into and , and the red signature is used for non-prescription drugs

    Products, green proprietary labels for non-prescription drugs。

    6 the specification of the drug is the quantity contained in a drug formulation unit. Drug specifications are usually expressed in terms of

    Quantities, , mass (weight), quantity, etc. Are expressed in one or several combinations。

    7. Quality standards are national and technical requirements and are medicines

    Legal basis to be followed jointly by goods, uses, inspection and regulatory authorities。

    8. The duration of the life of the drug shall be defined as the period during which the drug shall be of good quality under certain conditions and shall be based on stability

    The results of sexual tests and sampling are reasonably designed ... The duration of a generic drug can be expressed。

    9 distinction between and depending on the shape and hardness of the capsule.

    Drug knowledge test papers and answers

    10. The most fundamental difference between health-care foods and medicines is that health-care foods have no precise effect and cannot be used

    Prevention and treatment of diseases, with only functions, i. E. Non-propagating therapeutic efficacy.

    The operation of type ii psychopharmaceuticals is subject to strict double control. Dedicated books and related records, security instruments

    It's been in the last year of life.

    Ii. Questions of judgement (two points each, 20 points)

    A. Non-prescription drugs must be purchased and used at pharmacies under the direction of a practising pharmacist (...)

    2. Same drug, different types of agent, same speed, intensity and duration. ( )

    The release within 12 hours of the release of the tablets was measured at equal speed and the blood levels remained relatively stable. ( )

    4. Releases at the beginning of the slow release tablets are relatively rapid and have better effects; over time the release rate is slowing down and the efficacy of the drug is decreasing

    Weak. ( )

    5. Approval of medicines is the state's approval of the production of medicines by drug-producing enterprises and is a sign of the legitimacy of drug production. Not

    Medicines produced with the approval of a symbol are subject to a counterfeit drug. ( )

    6. Drug trade names may not be cross-written with generic names, and their fonts and colours may not be more prominent and visible than common names

    The font shall not exceed one third of the font used for the common name. ( )

    7. Drugs valid until 2015. 04 are valid until 30/04/2015, from 05/2015

    Question 1 and answer for basic drug training - page 1

    Question 1 and answer for basic drug training - page 2

    Not valid since 01.()

    The expiry date of the drug is the date on which the drug cannot be used, if the expiry date is 2015. 04 medicine, the drug from

    Effective 1 march 2015. ( )

    Letter meaning of drug approval symbol h (chemicals), z (medium drugs), b (health products), s (biological products), t

    Drug knowledge test papers and answers

    (in vitro diagnostic drugs), f (medicine supplements), j (import of sub-medicine). ( )

    10. Common names may be used as trademarks for registration. ( )

    Iii. Optional topics (2 points per issue, 40 points)

    1. The first step in starting a pharmaceutical business ()

    Legal personality b, operating licence c, pharmaceutical licence d, health clearance evidence

    2. Drugs under special state management are available. 1 cancer drug 2 narcotic drug 3 serum vaccine 4 psychotropic drug

    5 radiopharmaceutical 6 toxics

    A. 2345b. 3456c. 2456d. 1234

    3. Under the regulations on the regulation of medicines and labelling (decree no. 24), the name of the drug shall not correspond to the common name

    Peer writing, whose fonts and colours may not be more prominent and visible than the common name, and whose fonts may not be greater than that of general use by word area

    Font(s) used for names

    A, 1/4b, 1/2c, 1/3d, 1/5

    The internal label of the drug shall include the generic name of the drug, the subject matter of adaptability or function, the specification, the amount of use used, the date of production, and the date of production

    Product number, period of validity, production enterprise, etc. Indicators

    Note generic drug name, specifications and () content。

    A. Product number b, production enterprise c, usage d, validity period

    5. Which of the following cases are counterfeit ()

    A. B in excess of the validity period, c in deterioration, d without the approval symbol, d without the production lot number

    6. Which of the following cases are considered poor ()

    A. B in excess of the validity period, c in deterioration, d in non-validity, no production lot number indicated

    7. The correct management of the return of drugs after sale is:

    Drug knowledge test papers and answers

    A. Receipt of b on return notice from operations, strict inspection of packaging and acceptance of quality

    C. Two-person management area in d

    8. The following are subject to prescription sales ()

    A, chlorpropylene b, libavirin particle c, cyclophosphate d, gastrogen digestion snippets

    Persons suffering from any of the following diseases are prohibited from direct access to medicines. ( )

    A, b, diabetes c, hypertension d, gout

    10. The marking on the amosilin capsule is valid until march 2014 and the drug expires ()

    A, 1 april 2014 b, 28 february 2014 c, 31 march 2014 d, 1 march 2014

    11. Drugs and walls are not less than ()

    A, 10 cm b, 20 cm c, 30 cm d, 50 cm

    Question 1 and answer for basic drug training - page 2

    Question 1 and answer for basic drug training - page 3

    12. The temperature of storage of a drug shall be: ()

    A, under 30 degrees b, 2-8 degrees c, under 20 degrees d, under 25 degrees

    13. What proof must be obtained from the supplier(s) for the purchase of imported medicines by pharmaceutical producers, operators and users ()

    A. Copies of certified production certification from producing countries with original seals on supply units

    B. Copies of certification documents approved for listing by producing countries with original seals on supply units

    C. Copies of imported medicines registration certificate with original seal of the supplier unit

    D. A copy of the import drugs customs request, indicating “a sampled and stamped supply units”

    14. The scope of the measures for the regulation of drug circulation control is to be applied by units or individuals in the people's republic of china.

    A. Production of drugs b, purchase and sale of drugs c, use of drugs d, supervision of medicines

     
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