Professional Documents
Culture Documents
Instructions to candidates:
A. I and II only
B. I and Ill only
C. Ill and IV only
D. None of the above
A I and II only
B. II and IV only
C. Ill and IV only
D. All of the above
5. According to the Sale of Drugs Act 1952 and its regulations, medicinal
purpose includes·
I. diagnosis of a disease.
II. relieving pain.
Ill. anaesthetic.
IV. arbotifacient.
6. According to the Sale of Drugs Act 1952 and its regulations regarding
cosmetics, an exemption may be applied for
A. I and II only
B. Ill only
C. Ill and IV only
D. All of the above
A. I and II only
B. II and Ill only
C. Ill and IV only
D. None of the above
9. According to the Dangerous Drugs Act 1952 and its regulations, manufacture
of a drug or drug preparation includes the act of
I. producing.
II. transforming.
Ill. compounding.
IV. refining.
A. I and II only
B. II and Ill only
C. Ill and IV only
D. All of the above
I. The required entry must be made on the day in which the drug or
preparation is transacted without any delay allowed.
II. A registered dentist who enters details of the transaction in a day-book
and a reference in a separat~ book is exempted from keeping the
Register as set out in the Second Schedule.
Ill. A licenced retail seller of Part I Poisons may enter in the Register a
reference of the transaction as in the Prescription Book.
IV. The master of any ship may enter in the ship's official log book.
11 . For Malaysia, the Good Governance for Medicine (GGM) initiative is most
closely related to the
12. According to the Good Governance for Medicine (GGM) initiative, the
following statement is TRUE of weaknesses related to any drug selection
committee of hospital:
A. I and II only
B. II and Ill only
C. Ill and IV only
D. All of the above
I. Provide accurate and current information for which they are qualified in
their area of competence and within their scope of practice.
II. Aware of the limitations of their knowledge and skills and refer patients
to appropriate health care professionals when they are unable to meet
the needs of their patients.
Ill. Establish personal relationship with the patient as a moral obligation.
IV. Respect the autonomy of patients with diminished competence in
decisions regarding their health.
15. With reference to the Code of Conduct for Pharmacists and Bodies Corporate,
the following act is considered derogatory to the reputation of the profession:
18. The following is an offence under Regulation 18A(1) Control of Drugs and
Cosmetics Regulations 1984:
19. Persons appointed under the Sale of Drugs Act 1952 include:
I. Officer
II. Inspector
Ill. Drug Enforcement Officer
IV. Analyst
A. I and II only
B. I, II and IV only
C. II and Ill only
D. All of the above
A. I and II only
B. I, II and Ill only
C. Ill and IV only
D. All of the above
21. The following statement is TRUE regarding the Medicines (Advertisement and
Sale) Act 1956 and its regulations:
22. The sale and supply of the following is under the control of the Dangerous
Drugs Act 1952 and its regulations:
A. I and II only
B. I, II and IV only
C. II and IV only
D. All of the above
I. Powdered form
II. Unregistered product
Ill. Flavoured syrup
IV. Registered product
24. With reference to the Registration of Pharmacists Act 1951 and its
regulations, the investigation on a complaint against a registered pharmacist
received by the Secretary of the Pharmacy Board is conducted by the
I. Pharmacy Board.
II. Committee of Inquiry appointed by the Pharmacy Board.
Ill. Inspector appointed under Section 21 of the Act.
IV. Disciplinary Committee of the Pharmaceutical Service Division.
A. I and II only
B. I, II and IV only
C. Ill and IV only
D. None .ofthe above
25. With reference to the Registration of Pharmacists Act 1951 and its
regulations, the following statement is TRUE regarding a Provisionally
Registered Pharmacist:
A. I and II only
B. I, II and Ill only
C. I and Ill only
II D. All of the above
I i
A. I only
B. I, II and Ill only
C. I and IV only
D. II and Ill only
27. The import authorization is required under the Dangerous Drugs Act 1952 for
the following item
I. Codeine tablet
II. Pethidine injection
Ill. Tramadol tablet
IV. Diphenoxylate tablet
A. I and II only
B. I, II and IV only
C. Ill and IV only
D. All of the above
A. I and II only
B. I, Ill and IV only
C. I and IV only
D. II and IV only
A. I only
B. I and Ill only
C. II and IV only
D. All of the above.
30. The Drug Control Authority may issue the following licence:
I. Import licence
II. Clinical trial import licence
Ill. Manufacturer's licence
IV. Wholesaler's licence
A. I and II only
B. I, Ill and IV only
C. II only
D. None of the above
I. Regulation 7(1)(b)
II. Regulation 12(b)
IIIII Ill. Regulation 12(d)
IV. Regulation 21(1)
A. I and II only
B. I and Ill only
C. I, Ill and IV only
D. Ill and IV only
I. An authorized officer
II. A Drug Enforcement Officer
Ill. A registered pharmacist in public services
IV. Any offi~r of the Ministry of Health
A. I only
B. I and Ill only
C. II and IV only
D. All of the above
A. I only
B. I, II and Ill only
C. I and IV only
D. None of the above
I. Diazepam
II. Sulphinpyrazone
Ill. Oxyphenbutazone
IV. Nimetazepam
A. I and II only
B. I and IV only
C. II, Ill and IV only
D. All of the above
I. imported.
II. exported.
Ill. manufactured.
IV. supplied by wholesale.
A. I and II only
B. I and Ill only
C. I, Ill and IV only
D. II and IV only
A. I and II only
B. I, II and Ill only
C. Ill and IV only
D. All of the above
39. Any breach of the ·Code of Conduct for Pharmacists and Bodies Corporate
2009 shall be deemed in opinion of the Board as misconduct of a
I. Licenced pharmacist
II. Registered pharmacist
Ill. Superintendent
IV. Registered body corporate
A. I and II only
B. II only
C. Ill and IV only
D. IVonly
40. With reference to the Code of Conduct for Pharmacists and Bodies Corporate
2009, abuse of professional privileges and skill refer to
I. accountability.
II. compliance of policy.
Ill. abuse of confidence.
IV. undue influence.
A. I and II only
B. I, Ill and IV only
C. Ill only ·
D. All of the above
A. I and II only
B. I and IV only
C. II, Ill and IV only
D. All of the above·
A. I and II only
B. I, II and IV only
C. II and Ill only
D. All of the above
43. The Public Prosecutor may authorize in writing such persons to conduct
prosecutions in respect of offences under the Poisons Act 1952:
A. I and II only
B. I, II and Ill only
C. II, Ill and IV only
D. All of the above
A. lonly
B. I, II and Ill only
C. II and Ill only
D. All of the above
45. Under the relevant pharmacy legislations, the following persons shall keep
and maintain a register to be called the "Register of Psychotropic Substance
Received, Delivered or Administered".
A. I and II only
B. I and Ill only
C. Ill and IV only
D. All of the above
46. The Minister may make regulations under the Sale of Drugs Act 1952 for the
following purpose to
A. I only
B. I and II only
C. II only
D. II, Ill and IV only
48. Under the Control of Drugs and Cosmetics Regulations 1984, the Director of
Pharmaceutical Services may issue written such directives or guidelines to
any person or a group of persons which in particular relate to
A. I and II only
B. I, Ill and IV only
C. II and Ill only
D. All of the above
49. Under the Control of Drugs and Cosmetics Regulations 1984, a register of the
products registered, kept and maintained by the Secretary shall contain
A. I and tl only
B. II and IV only
C. I, II and Ill only
D. All of the above
51. The following persons shall be the members in the establishment and
constitution of the Pharmacy Board:
A. l .and II only
B. II and Ill only
C. II, Ill and IV only
D. All of the above
52. Under the Registration of Pharmacists Act 1951, the Board may make
regulations for and in respect of all or any of the following matters:
A. I only
B. II, Ill and IV only
C. II and IV only
D. All of the above
54. The following person may conduct prosecution in respect of any offences
under the Dangerous Drugs Act 1952 and its regulation.
A. I and II only
B. II and Ill only
C. II, Ill and IV only
D. All of the above
55. Quality Use of Drugs shall be achieved by promoting rational prescribing and
II appropriate use of medicines by consumers through
A. I and II only
B. II and Ill only
C. Ill and IV only
D. All of the above
A. I and II only
B. I, II and Ill only
C. II and Ill only
D. All of the above
57. The following statement is TRUE regarding the requirement for the
importation of cosmetic:
I. The importer shall be the person responsible for placing the notified
cosmetic in the market or a person authorized in accordance with the
notification note.
II. The cosmetic shall be notified with the Drug Control Authority.
Ill. The importer shall have an import licence issued under the Control of
Drugs and Cosmetics Regulations 1984.
IV. The importer shall have a licence issued under the Poisons Act 1952.
A. I only
B. I, II and IV.only
C. II and Ill only
D. All of the above
58. Under the Control of Drugs and Cosmetics Regulations 1984, the following
activity requires a written approval by the Director of Pharmaceutical Services:
A. I and II only
B. I, Ill and IV only
C. Ill and IV only
D. All of the above
A. I and II only
B. I, II and Ill only
C. Ill and IV only
D. All of the above
60. Under the Control of Drugs and Cosmetics Regulations 1984, a licenced
manufacturer shall
A. I and II only
B. I, Ill and IV only
C. II , Ill and IV only
D. All of the above
61. The following is a requirement under the Dangerous Drugs Regulations 1952,
regarding a registered product containing Pholcodeine:
I. The related records shall be preserved for a period of two years from
the date on which the last entry is made therein.
II. The prescription issued shall be preserved for a period of three years
from the date on which it is issued .
Ill. Every drug used in manufacturing shall be entered in the Register.
IV. Supply by way of wholesale dealing shall be by a person duly
authorized by a "Licence To Keep And Sell Dangerous · Drugs By
Wholesale"
63. The following poison may be supplied by a registered medical practitioner for
the medical treatment of his patient:
I. Carbadox
II. Clioquinol
Ill. Cetirizine
IV. Cetrorelix
A I and II only
B. I, II and IV only
C. Ill and IV only
D. All of the above
64. Under the Poisons Act 1952 and its regulations, the Drug Enforcement Officer
may
A I and II only
B. I, II and Ill only
C. Ill and IV only
D. All of the above
66. The following statement is TRUE regarding the meeting of the Medicine
Advertisements Board (MAB):
I. The Director General of Health shall be the Chairman of the MAB and
shall preside at all meetings which he attends.
II. In the absence of the Chairman from any meeting the members
present shall elect one of their members to preside.
Ill. The MAB may invite any person to attend any meeting of the MAB.
IV. · The quorum of the meeting is four including the Chairman.
67. The following statement is TRUE regarding Registrar under the Registration
of Pharmacists Act 1951:
A I and II only
B. II, Ill and IV only
C. Ill and IV only
D. All of the above
A. I and II only
B. I and IV only
C. Ill and IV only
D. IVonly
A. I and II only
B. I, II and Ill only
C. Ill and IV only
D. All of the above
73. The following statement is TRUE regarding the Medicines (Advertisement and
Sale) Act 1956:
A. I and II only
B. I and Ill only
C. II, Ill and IV only
D. II and IV only
I. May enter and inspect any place where there is any drug intended for
sale
II. May seize any drug which is unwholesome or deleterious to health
Ill. Any public servant may be appointed as officer and inspector
IV. Certificate of analysis issued by the officer and inspector is a prima
facie evidence
75. The following statement is TRUE pertaining the proceedings for offences
under the Sale of Drugs Act 1952:
A. The summons to the accused is served less than 14 days before trial
B. To be carried only before Magistrate Court
C. May be instituted more than sixty days from the time of any article of
drug has been purchased or procured for the test purposes
D. Certificate of analysis by the analyst to be prima facie evidence
76. The following statement is TRUE regarding the Secretary of the Pharmacy
Board:
A. I and II only
B. II and IV only
C. Ill and IV only
D. JVonly
78. The following is a TRUE statement regarding members of the Poisons Board:
I. All members other than the Director General of Health are appointed
by the Minister.
II. The Director of Pharmaceutical Services is the ex-officio member.
Ill. The Minister may, after consultation with the Board, appoint a
Secretary who shall not be a member.
IV. The Board may appoint a person to be a temporary member who shall
be deemed to be a member of the Board.
A. I and II only
B. I and Ill only
C. I, Ill and IV only
D. All of the above
79. The following is a TRUE statement regarding the meeting of the Poisons
Board:
I. The Director General of Health shall be the Chairman and shall preside
at all meeting he attends.
II. The Director of Pharmaceutical Services is the alternate Chairman.
Ill. The Board may invite any one or more persons to attend any meeting
of the Board.
IV. At any meeting, four members including the Chairman shall form a
quorum.
82. The following person may compound or mix any poison with other substance,
for the purpose of it being used for medical treatment:
I. A registered pharmacist
II. A licenced pharmacist
Ill. A registered medical practitioner
IV. A registered dentist Division I
A. I, II and Ill only
B. I and Ill only
C. Ill and IV only
D. All of the above
84. Under the Poisons Act 1952, a Type B licence holder may sell as wholesale
Hydrochloric Acid 25% to
85. Under the Poisons Act 1952, a licenced pharmacist may sell by retail the
following poison as a dispensed medicine in accordance with a prescription
prescribed by a registered medical practitioner:
I. Group A poison
II. Group B poison
Ill. Medicine containing psychotropic substances
IV. Group C poison
A. I and II only
B. II, Ill and IV only
C. Ill and IV only
D. All of the above
87. The following statement is TRUE regarding the appointment of the members
of the Pharmacy Board:
A. I and II only
B. I and IV only
C. Ill and IV only
D. None of the above
A. I and II only
B. I and Ill only
C. Ill and IV only
D. IVonly
With reference to the Registration of Pharmacists Act 1951- & its regulations,
Professor Z may be appointed as
90. The following statement is TRUE regarding the Sale of Drugs Act 1952:
A. I and II only
B. I and Ill only
· C. II and IV only
D. Ill and IV only
I. The business of such body corporate shall be under the control and
management of a superintendent who is a registered pharmacist.
II. Any body corporate that having more than one premise, each of the
premises shall be managed by a separate superintendent.
Ill. A copy of the registration certificate of the superintendent shall be
conspicuously exhibited in each premise if such body corporate is
having more than one premise.
IV. The superintendent shall be a citizen of Malaysia.
A. I and II only
B. I and Ill only
C. II and IV only
D. All of the above
93. The following statement is TRUE regarding licences under the Control of
Drugs and Cosmetics Regulation 1984:
I. Part I poison
II. Group B poison
Ill. Part II poison
IV. Group C poison
A. I and II only
B. I and IV only
C. II and Ill only
D. Ill and IV only
I. A vape vendor
II. Division II Dentist
Ill. A registered nurse
IV. A medical sales representative
A. I only
B. II and Ill only
C. I, II and Ill only
D. All of the above
I II
97. The following statement is FALSE regarding the implementation of Good
Governance for Medicine:
99. The following statement is FALSE on clinical trial as stipulated under Control
of Drugs and Cosmetics Regulations 1984:
A. I, II and IV only
B. I and Ill only
C. II, Ill and IV
D. All of the above