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Free Practice Questions for Pharmacist Evaluating Exam

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Key Facts: Pharmacist Evaluating Exam Exam

70

Multiple-choice questions on the written paper administered by the Mauritius Examinations Syndicate (MES)

Pharmacy Council of Mauritius Syllabus (2024) and Model Exam Paper

50 / 100

Minimum marks required to pass the overall examination (70% written + 30% viva/project)

Pharmacy Council of Mauritius Syllabus (2024), page 4

1 year

Minimum duration of approved pre-registration practical training required before taking the exam

Pharmacy Council Act 2015, Section 18(1)(d)

21 points

Minimum A-Level points (any 3 subjects at one sitting) required for registration as a pharmacist or pre-registration trainee

Pharmacy Council Act 2015, Section 18(1)(b)

3 years

Foreign practice experience required for exam exemption under Section 18(2)(c)

Pharmacy Council Act 2015, Section 18(2)(c)

9 points

Minimum annual CPD credit points required for registered pharmacists in subsequent years

Pharmacy Council (CPD) Regulations 2018, Regulation 3(1)

To register as a pharmacist in Mauritius under the Pharmacy Council Act 2015, pre-registration trainees must pass the Pharmacist Evaluating Examination: a 70-mark written MCQ paper administered by the Mauritius Examinations Syndicate (MES) plus a 30-mark viva voce and project presentation, with an overall pass mark of 50/100. This free, independent practice bank provides 100 practice questions covering the Pharmacy Laws, Pharmacy Practice, and Miscellaneous sections of the official 2024 syllabus. It is an MCQ study aid for the written paper, not a simulation of the viva voce or project presentation.

Sample Pharmacist Evaluating Exam Practice Questions

Try these sample questions to review concepts for the Pharmacist Evaluating Exam exam. Each question includes a detailed explanation. Start the interactive quiz above for the full 100+ question experience with AI tutoring.

1Under section 3 of the Pharmacy Act 1983, which of the following correctly describes the Pharmacy Board and its Registrar?
A.The Chief Medical Officer as Chairman, the Chief Government Pharmacist, 5 pharmacists appointed by the Minister and a law officer designated by the Attorney-General, with a Government Pharmacist designated by the Minister acting as Registrar
B.The Chief Medical Officer as Chairman, the Chief Government Pharmacist, 3 pharmacists appointed by the Minister and a law officer designated by the Attorney-General, with a Government Pharmacist designated by the Minister acting as Registrar
C.The Chief Government Pharmacist as Chairman, the Chief Medical Officer, 5 pharmacists elected by registered pharmacists and a law officer, with the Registrar of the Pharmacy Council acting as Registrar
D.The Chief Medical Officer as Chairman, 5 pharmacists appointed by the Minister and a law officer, with the Chief Government Pharmacist acting as Registrar instead of sitting as a member
Explanation: Section 3(1) of the Pharmacy Act 1983 sets the Board as the Chief Medical Officer (Chairman), the Chief Government Pharmacist, 5 pharmacists appointed by the Minister and a law officer designated by the Attorney-General. Section 3(2) adds that a Government Pharmacist designated by the Minister acts as Registrar of the Board. The Council's model paper summarises this as the CMO, the Chief Pharmacist, 5 pharmacists, a law officer and a Registrar.
2According to section 18(1) of the Pharmacy Act 1983, under what legal conditions may a person operate a retail pharmacy in Mauritius?
A.Solely upon obtaining a commercial trade licence from the local municipal council
B.Provided the business owner holds a degree in pharmaceutical sciences, regardless of physical supervision
C.Only if the owner is registered as a medical practitioner with the Medical Council of Mauritius
D.Only if he holds a pharmacy licence issued by the Board and there is a registered pharmacist in charge
Explanation: Section 18(1) of the Pharmacy Act 1983 provides that no person shall operate a pharmacy unless he holds a licence and there is a pharmacist in charge of the pharmacy. The licence is granted by the Pharmacy Board, is valid for one year and is renewable annually (section 18(7)). Section 17 deals with what may be sold in a pharmacy, not with who may operate one.
3How does the interpretation section (section 2) of the Pharmacy Act 1983 define the 'temporary absence' of a pharmacist?
A.A single period not exceeding 4 consecutive hours in a week
B.A period of absence not exceeding 2 hours in a single day
C.An absence not exceeding 1 hour in the morning and 1 hour in the evening
D.A total absence not exceeding 3 hours per working day
Explanation: Section 2 of the Pharmacy Act 1983 defines 'temporary absence' as any period of absence not exceeding two hours in a day. The definition matters because, during such an absence, an assistant pharmacist may keep the Prescription Book (section 20(1)) and dispensing may take place in his presence (section 18(9)).
4Where a dispensing pharmacist considers that an authorised prescriber has made an evident error on a medical prescription, what is the pharmacist's legal obligation under Section 21 of the Pharmacy Act 1983?
A.Immediately dispense an alternative lower dose without contacting the prescriber
B.Delay the execution of the prescription and refer the matter immediately to the prescriber for confirmation
C.Dispense the medication as written and notify the Ministry of Health after 48 hours
D.Cancel the prescription and return it to the patient with instructions to consult another doctor
Explanation: Section 21(2) of the Pharmacy Act 1983 provides that where the pharmacist considers that the authorised person has made an evident error, or overlooked something which may endanger the life or health of the patient, he shall delay the execution of the prescription and refer the matter immediately to that person for confirmation.
5According to Section 20(2) of the Pharmacy Act 1983, for what minimum duration must a Prescription Book be retained in the pharmacy following the date of the last entry?
A.1 year from the date on which the last prescription is entered
B.2 years from the date on which the last prescription is entered
C.3 years from the date on which the last prescription is entered
D.5 years from the date on which the last prescription is entered
Explanation: Section 20(2) of the Pharmacy Act 1983 explicitly provides that the Prescription Book shall be kept on the pharmacy premises for a period of 2 years from the date on which the last prescription is entered.
6Under Section 33 of the Pharmacy Act 1983, every person who sells or supplies an antibiotic is required to maintain which record, and for what minimum retention period?
A.An Antibiotic Book, kept on the premises for a period of 2 years from the date of the last entry
B.A General Poison Register, kept on the premises for a period of 1 year from the date of sale
C.An Electronic Requisition Ledger, kept for 5 years from the date of initial entry
D.A Therapeutic Substances Pad, retained for 6 months from the date of dispensing
Explanation: Section 33(1) and (2) of the Pharmacy Act 1983 requires every person who sells or supplies a therapeutic substance that is an antibiotic to keep an Antibiotic Book and record every sale and supply, keeping the book on premises for 2 years from the date of the last entry.
7Which function belongs to the Trade and Therapeutics Committee (TTC) under the Pharmacy Act 1983?
A.Hearing disciplinary complaints of professional misconduct against registered pharmacists and recommending sanctions
B.Setting retail profit margins and customs tariffs for imported pharmaceutical products each year
C.Advising the Pharmacy Board on the manufacture and importation of pharmaceutical products, including product-registration applications
D.Supervising the pre-registration training of pharmacy graduates at Council-approved training sites
Explanation: Section 7 of the Pharmacy Act 1983 sets up the TTC to advise the Board on the manufacture and importation of pharmaceutical products, the National Drugs Formulary, reported adverse drug effects and areas needing a pharmacy. Under section 25(3) the Board refers every product-registration application to the TTC for its recommendations. Under section 18(3) the TTC also inspects premises proposed for a new pharmacy.
8Under section 8 of the Pharmacy Act 1983, what is the role of the Poisons Committee?
A.To advise the Board on applications to build a factory to manufacture pharmaceutical products
B.To advise the Board on the compilation and maintenance of the National Drugs Formulary
C.To advise the Board on any matter relating to poisons, dangerous drugs and psychotropic substances
D.To grant licences to persons who wish to operate a pharmacy
Explanation: Section 8(1) of the Pharmacy Act 1983 establishes the Poisons Committee to advise the Board on any matter relating to poisons, dangerous drugs and psychotropic substances. It is chaired by the Chief Government Pharmacist. Under section 27(8) the Board also asks it to examine applications for a licence to sell poisons.
9Under section 29 of the Pharmacy Act 1983, what must a seller do when selling a poison specified in the Fifth Schedule, and how long must the Poisons Book be kept?
A.Cause the purchaser to sign an entry in the Poisons Book before the poison is delivered (or accept a qualifying signed order), and keep the book on the premises for 2 years from the last entry
B.Make an entry in the Poisons Book within 7 days after the poison is delivered, and keep the book on the premises for 1 year from the last entry
C.Record the sale only in the Prescription Book kept under section 20, which is retained for 2 years, since poisons need no separate register
D.Obtain the written approval of the Poisons Committee before each sale, and keep every approval on the premises for 5 years from its date
Explanation: Section 29(1) requires every person who sells a First or Fifth Schedule poison to keep a Poisons Book. For a First Schedule poison the seller makes the entry before delivery; for a Fifth Schedule poison the purchaser must sign the entry before delivery. The book is kept on the premises for 2 years from the last entry. Section 29(2) allows a signed order containing the purchaser's details, quantity and purpose instead of a signature, marked 'signed order' in the book.
10On the death of the pharmacist in charge of a pharmacy, what does section 19 of the Pharmacy Act 1983 allow the licensee (or the deceased pharmacist's spouse or heirs) to do, with the Board's approval?
A.Operate the pharmacy under the direct management of an assistant pharmacist for up to 3 months, followed by supervision by another pharmacist for a further 8 days
B.Operate the pharmacy under the direct management of an assistant pharmacist for up to 8 days, then have it supervised by a pharmacist already in charge of another pharmacy for a further period of up to 3 months
C.Continue the business for up to 3 years under the continuous management of a registered pharmacist
D.Continue trading without any pharmacist until the estate is settled, provided dangerous drugs are not sold
Explanation: Section 19(a) of the Pharmacy Act 1983 allows, with the Board's approval, operation under an assistant pharmacist for a period not exceeding 8 days. The pharmacy may then be supervised by a pharmacist already in charge of another pharmacy for a further period not exceeding 3 months. Where no pharmacist or assistant pharmacist can take charge, section 19(b) requires the stock to be sold to another pharmacy within a time set by the Board. Dangerous drugs are placed under seal by the Board.

About the Pharmacist Evaluating Exam Exam

The Pharmacist Evaluating Examination (also referred to on official materials as the Pharmacist Registration Examination or Examination for Pre-Registered Pharmacists) is the statutory exit examination established under Section 18(1)(e) of the Pharmacy Council Act 2015 for registration as a pharmacist in Mauritius. Conducted by the Mauritius Examinations Syndicate (MES) and the Pharmacy Council, the examination evaluates knowledge in pharmacy laws (Pharmacy Act 1983, Dangerous Drugs Act 2000, Pharmacy Council Act 2015, Code of Practice 2021, and IP laws), pharmacy practice (dispensing, bookkeeping, patient safety, applied pharmacology, pharmaceutics), and miscellaneous topics. OpenExamPrep provides free, independent practice questions for the written component.

Exam sponsor: Pharmacy Council of Mauritius, with written paper administration by the Mauritius Examinations Syndicate (MES). The requirements and fees below concern the certification or admission exam, separate from our free practice resources.

Assessment

The assessment comprises two components: a written examination consisting of 70 single-response multiple-choice questions (carrying 70 marks, 70% of total) conducted by the Mauritius Examinations Syndicate (MES), and an oral viva voce examination (carrying 30 marks / 30% of total, split into a 25-mark viva and 5-mark project presentation before a designated Council panel). The written paper covers Pharmacy Laws (30 marks), Pharmacy Practice (30 marks), and Miscellaneous topics (10 marks).

Time Limit

not-published

Passing Score

50 / 100 marks (50%)

Exam / Certification Fees

not-published

Exam sponsor website

Fees, eligibility, and exam policies can change. Confirm them with the exam sponsor before applying or paying.

Official sources

Our practice resources: topics covered

We aim to reflect publicly available exam outlines and topic information in our study resources. Coverage, format, and difficulty may differ from the actual exam, and we cannot guarantee that every detail is accurate or current. Confirm exam requirements, fees, and policies with the official exam sponsor.

30 marks (written paper)

The Pharmacy Laws

Statutory provisions of the Pharmacy Act 1983, Dangerous Drugs Act 2000, Pharmacy Council Act 2015, CPD Regulations 2018, Code of Practice Regulations 2021, and Mauritian intellectual property legislation.

30 marks (written paper)

The Pharmacy Practice

Pharmacy bookkeeping (DD, antibiotic, and poison registers; prescription book), prescription evaluation, dosage calculations, patient safety, applied pharmaceutics, clinical pharmacology, veterinary products, wholesale operations, hospital management, and waste disposal.

10 marks (written paper)

Miscellaneous

Clinical toxicology, local drug addiction epidemiology and harm reduction, pharmaceutical care principles, Data Protection Act 2017, anti-doping legislation, clinical trials legislation, consumer protection, and research methods.

Preparing for the Pharmacist Evaluating Exam Exam

What You Need to Know

  • Passing score: 50 / 100 marks (50%)
  • Assessment: The assessment comprises two components: a written examination consisting of 70 single-response multiple-choice questions (carrying 70 marks, 70% of total) conducted by the Mauritius Examinations Syndicate (MES), and an oral viva voce examination (carrying 30 marks / 30% of total, split into a 25-mark viva and 5-mark project presentation before a designated Council panel). The written paper covers Pharmacy Laws (30 marks), Pharmacy Practice (30 marks), and Miscellaneous topics (10 marks).
  • Time limit: not-published
  • Exam / certification fees: not-published Official sources

Using Our Practice Resources

  • Work through all 100 available questions
  • Review every answer and explanation
  • Track weak areas and revisit them
  • Use our AI tutor for tough concepts

Pharmacist Evaluating Exam: Suggested Study Strategy

1Master the exact statutory time limits and retention periods: 2 years for the Prescription Book and Antibiotic Book under the Pharmacy Act 1983, and 5 years for Dangerous Drugs Act 2000 records.
2Learn the Dangerous Drugs Act prescribing limits as amended in 2022: 14 days of treatment for Schedule II (and specified Schedule III) drugs and one month for other Schedule III drugs. Older copies of the Act still print 10 days.
3Familiarize yourself with the composition and specific mandates of the Pharmacy Board, the Pharmacy Council of Mauritius, and the Disciplinary Tribunal under the respective Acts.
4Practice standard paediatric dosage calculations using Clark's Rule (weight in lbs), Young's Rule (age in years), Friend's Rule (age in months), and Body Surface Area nomograms.
5Review Mauritian pharmaceutical waste disposal guidelines, distinguishing items requiring high-temperature incineration from those suitable for Mare Chicose landfill or sewer dilution.

Frequently Asked Questions

What is the Pharmacist Evaluating Examination in Mauritius?

The Pharmacist Evaluating Examination (also called the Pharmacist Registration Examination or Examination for Pre-Registered Pharmacists) is the mandatory statutory licensing examination conducted under Section 18(1)(e) of the Pharmacy Council Act 2015. It evaluates whether pre-registration pharmacy trainees who have completed at least one year of approved training possess the requisite legal and clinical competencies to practice as registered pharmacists in Mauritius.

What is the structure, question count, and pass mark of the examination?

The examination is weighted out of 100 total marks: a 70-mark written examination consisting of 70 multiple-choice questions administered by the Mauritius Examinations Syndicate (MES) and a 30-mark viva voce examination (comprising a 25-mark oral assessment and a 5-mark project presentation before a Pharmacy Council panel). The overall passing score is a minimum of 50 marks out of 100.

How much is the examination fee?

The examination fee has not been publicly specified in published regulations; the Pharmacy Council's official examination page notes that payment modalities will be communicated directly to candidates prior to the examination. Separate administrative fees set under the Pharmacy Council Regulations 2017 include Rs 1,000 for pre-registration trainee registration and Rs 2,000 for initial pharmacist registration.

Who is eligible to take the examination, and who is exempt?

Candidates need a pharmacy degree, diploma or equivalent from a full-time course of at least 4 years, and passes in any 3 A-Level subjects at one sitting with at least 21 points (or an approved equivalent). They must also be registered as pre-registration trainees and complete at least one year of approved pre-registration training at a Council-approved site. Under section 18(2)(c) of the Pharmacy Council Act 2015, a holder of such a qualification who is registered as a pharmacist by the regulator of the country where it was obtained, with at least 3 years' experience as a pharmacist, is exempt.

What topics are covered on the written paper?

The 70-question written paper follows the syllabus published by the Pharmacy Council of Mauritius: Pharmacy Laws carries 30 marks, Pharmacy Practice carries 30 marks, and Miscellaneous topics carries 10 marks.

Is this practice bank affiliated with the Pharmacy Council of Mauritius?

No. OpenExamPrep provides free, independent study questions to assist candidates preparing for the written paper and legal knowledge areas. It is not an official Pharmacy Council of Mauritius or MES examination paper and does not simulate the oral viva voce or project presentation.