Pharmaceutical Administration and Regulations Mock Exam Questions and Answers for Practicing Pharmacists (6)

14. According to the "Good Manufacturing Practices for Pharmaceutical Distribution", the first varieties of pharmaceutical operating enterprises refer to

A. Drugs imported for the first time in China

B. Domestic Drugs produced and put on the market for the first time

C. Drugs put on the market for the first time in the local area

D. Drugs purchased by the enterprise for the first time from a certain drug manufacturer

E. Drugs exported by this enterprise for the first time

Standard answer: d

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

A. One year

B. Two years

C. Three years

D. Four years

E. Five years

Standard answer: c

16. According to the "Regulations on the Management of Proprietary Labels of OTC Drugs (Interim)", the proprietary labels of OTC drugs that can be printed in a single color are:

A. Labels and Inner packaging

B. Instructions for use and large packaging

C. Labels and instructions for use

D. Inner packaging and large packaging

E. Labeling and large packaging

Standard answer: b

17. According to the requirements for drug storage temperature and humidity, which one is correct

A. Cold storage 2 to 10 ℃, relative humidity 45～75

B. Cold storage 2～10℃, relative humidity 25～75

C. Shade and cool storage ≤15℃, relative humidity 5～75

D. Normal temperature warehouse 0～30℃, relative humidity 25～75

E. Normal temperature warehouse 10～30℃, relative humidity 5～75

Standard answer: a

18. "Prescription Management Measures" applies to

A. Medical institutions and their personnel related to prescription issuance, dispensing, and preparations

B. Prescriptions Medical institutions and their personnel related to issuance, transfer, and storage

C. Medical institutions and their personnel related to prescription issuance, transfer, verification, and inspection

D. Prescription issuance, Medical institutions and their personnel related to dispensing, preparation, supervision and management

E. Medical institutions and their personnel related to prescription issuance, dispensing, clinical monitoring and testing

Standard answer: b

19. The "Prescription Management Measures" stipulates that the prescription format consists of three parts, of which the main text includes

A. Marked with Rp or R, the drug name, dosage form, and quantity are listed. , Usage

B. Prescription number, marked with Rp or R, listing drug name, dosage form, usage and dosage

C. Prescription number, marked with Rp or R, clinical diagnosis, List the drug name, specifications, and dosage

D. Mark it with Rp or R. List the drug name, dosage form, specification, quantity, usage and dosage

E. Clinical diagnosis, use Rp or R mark, listing the drug name, quantity, usage and dosage

Standard answer: d

20. According to the "Measures for the Supervision and Administration of Drug Circulation", drug manufacturers

A. Only over-the-counter drugs produced by the company can be sold

B. Prescription drugs produced by the company can only be sold

C. Prescription drugs produced by the company cannot be sold

D. Only the varieties produced by the company can be sold

E. The varieties produced by the company cannot be sold

Standard answer: d

21. By The circumstances in which the original issuing authority cancels the "Pharmaceutical Business License" do not include

A. The validity period of the "Pharmaceutical Business License" has expired and the license has not been renewed

B. The drug business enterprise terminates its operations Drugs may be closed

C. The "Pharmaceutical Business License" has been revoked, withdrawn, revoked, withdrawn and surrendered in accordance with the law

D. The "Pharmaceutical Business License" has been caused by force majeure

Licensing matters cannot be implemented

E. Violation of drug advertising regulations

Standard answer: e

22. According to the "Interim Provisions on the Qualification System for Practicing Pharmacists", practicing Implementation of pharmacist continuing education,

A. Assessment system

B. Examination system

C. 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 of the purchase and storage of drugs by medical institutions, The mistake is

A. When medical institutions purchase drugs, they must establish true and complete drug purchase records and store them directly in the warehouse

B. When storing drugs, medical institutions must first formulate and Implement systems related to the storage and maintenance of drugs

C. Medical institutions should store chemical drugs and proprietary Chinese medicines separately and in categories

D. Medical institutions shall not provide them directly to patients without diagnosis and treatment Drugs

E. Medical institutions are not allowed to sell prescription drugs directly to the public by mail

Standard answer: a

24. Fixed-point retail sales of urban employee basic medical insurance Prescriptions dispensed outside pharmacies should be kept

A. For more than 1 year for verification

B. For more than 2 years for verification

C. For more than 3 years for verification Verification

D. More than 4 years to prepare for verification

E. More than 5 years to prepare for verification

Standard answer: b

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

A. Participation in clinical drug trial program design

B. Participation in clinical drug treatment Plan design

C. Implement therapeutic drug monitoring for key patients

D. Collect drug safety information

E. Collect drug efficacy information

Standard answer: a

26. In accordance with the Price Law of the People's Republic of China, operators selling and purchasing goods and providing services must clearly mark their prices in accordance with regulations

, and indicate the product's

A. Product name, origin, specifications, grade, pricing unit, price, etc.

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

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

D. Product name, manufacturer, certificate, quality guarantee period, 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 Preparation Preparation in Medical Institutions ( Trial)", the items that should be stated in the "Medical Institution Preparation License" do not include

A. The person in charge of the preparation room

B. The person in charge of the drug testing room

　C. Preparation range

D. Preparation address

E. Validity period

Standard answer: b

28. According to " "Drug Instructions and Label Management Regulations", the following drug validity period marking format is wrong

A. Validity period until ×××year××month

B. Validity period until ××× ××年××月××日

C. Valid until ××××, ××

　D. Valid until ××××/××/××

E. Valid until ××/××/××××

Standard answer: e