A. Drugs imported from China for the first time

B. Drugs produced and sold in China for the first time

C, local drugs listed for the first time

D. Drugs purchased by this enterprise from pharmaceutical production enterprises for the first time.

E. Drugs exported by the enterprise for the first time

Standard answer: D.

15. According to the Interim Provisions on the Qualification System of Licensed Pharmacists, the validity period of registration of licensed pharmacists is

one year

It's been two years.

C, three years

D, four years

E, five years

Standard answer: C.

16 according to the regulations on the administration of over-the-counter special signs (provisional), over-the-counter special signs can be printed in monochrome.

I. Labels and inner packaging

B. Instructions for use and large package

C, labels and instructions for use

D, inner packaging and large packaging

Labels and large packages

Standard answer: b

17, which is correct according to the requirements of drug storage temperature and humidity.

First, the cold storage is 2 ~ 65438 00℃ and the relative humidity is 45% ~ 75%.

B, cold storage 2 ~ 65438 00℃, relative humidity 25% ~ 75%.

C, cold storage ≤ 15℃, relative humidity 5% ~ 75%.

D, the room temperature is 0 ~ 30℃ and the relative humidity is 25% ~ 75%.

E room temperature 10 ~ 30℃ and relative humidity 5% ~ 75%.

Standard answer: A.

18, prescription management measures apply to

I. Prescriptions, Dispensations and Preparations of Medical Institutions and Their Relevant Personnel

B, medical institutions and their personnel related to prescription, dispensing and storage.

C, medical institutions and their personnel related to prescription, dispensing, check and inspection.

D supervise and manage the prescriptions, dispensing and preparations of medical institutions and their personnel.

E prescription, dispensing, clinical monitoring and inspection related to medical institutions and their personnel.

Standard answer: b

19, the Prescription Management Measures stipulates that the prescription format consists of three parts, of which the text part includes

A, marked with Rp or R, indicating the drug name, dosage form, quantity and usage respectively.

B, prescription number, respectively marked with Rp or R, drug name, dosage form, usage and dosage.

C, prescription number, marked with Rp or R, clinical diagnosis, drug name, specification and dosage.

D, marked with Rp or R, indicating the drug name, dosage form, specification, quantity, usage and dosage respectively.

E, clinical diagnosis, marked with Rp or R, with drug name, quantity, usage and dosage respectively.

Standard answer: D.

20, in accordance with the provisions of the measures for the supervision and administration of drug circulation, drug production enterprises

1. Only the over-the-counter drugs produced by this enterprise can be sold.

B, can only sell prescription drugs produced by this enterprise.

C, can't sell prescription drugs produced by this enterprise.

D, only the varieties produced by this enterprise can be sold.

E, can't sell the varieties produced by this enterprise.

Standard answer: D.

2 1. The Drug Business License cancelled by the original issuing authority is not included.

1. The Drug Business License has not been renewed upon expiration.

B, pharmaceutical trading enterprises to terminate the drug business or shut down.

C the pharmaceutical trading license is revoked, withdrawn, revoked, withdrawn and cancelled according to law.

D. Force majeure causes the licensing items of the Drug Business License to be unable to be implemented.

E, in violation of the provisions of drug advertising

Standard answer: e

22, according to the "Interim Provisions" licensed pharmacist qualification system, licensed pharmacist continuing education,

I. Evaluation system

B. Examination system

C. Examination and approval system

D. Registration system

E. Registration system

Standard answer: D.

23. According to the Measures for the Supervision and Administration of Drug Circulation, the description about the purchase and storage of drugs by medical institutions is wrong.

First, medical institutions to buy drugs, must establish a true and complete drug purchase records, and directly into the warehouse.

B, medical institutions to store drugs, should first formulate and implement drug storage and maintenance system.

C, medical institutions should store and classify chemicals and proprietary Chinese medicines respectively.

D, medical institutions shall not directly provide drugs to patients without diagnosis and treatment.

E, medical institutions shall not directly sell prescription drugs to the public by mail.

Standard answer: A.

24, the basic medical insurance for urban workers designated retail pharmacies with prescription should be properly kept.

I. Check if it exceeds 1 year.

B, more than 2 years for verification.

C, more than 3 years for verification.

D, more than 4 years for verification.

E, more than 5 years for verification.

Standard answer: b

25, according to the "Interim Provisions on Pharmaceutical Affairs Management of Medical Institutions", the main responsibilities of clinical pharmacy professional and technical personnel do not include

First, participate in the design of clinical drug trial scheme

B, participate in clinical drug treatment scheme design

C, the implementation of therapeutic drug monitoring for key patients.

D, collecting drug safety information

E, collecting information on drug efficacy.

Standard answer: A.

26. According to the Price Law of People's Republic of China (PRC), business operators should clearly mark their prices to sell, buy goods and provide services.

Price, and indicate the goods.

1. Name, place of origin, specification, grade, unit of valuation, price, etc.

B, name, origin, specifications, certificate, use, price, etc.

C, name, manufacturer, specifications, certificate, validity period, price, etc.

D, product name, manufacturer, certificate, shelf life, price, etc.

E, product name, origin, certificate, performance, production cost, price, etc.

Standard answer: A.

27. According to the Measures for the Supervision and Administration of Preparations in Medical Institutions (for Trial Implementation), the items that should be specified in the Preparation License of Medical Institutions are not included.

First, the person in charge of the preparation room

Director of drug control room

C, preparation scope

D, prepare the address

E. Validity period

Standard answer: b

28. According to the Regulation on the Administration of Drug Instructions and Labels, it is wrong to label the following drugs in the format of expiry date.

1. The term of validity is * * * years.

B, valid until. }

C, valid until * * *, * *

D, valid until * */* */* *

E, valid until * */* * * *

Standard answer: e