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100+ Free State Medical Faculty Diploma in Pharmacy Final Exam Practice Questions

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2026 Statistics

Key Facts: State Medical Faculty Diploma in Pharmacy Final Exam Exam

3 years

Program Duration

SMFB & PCB curriculum

50%

Passing Score per Subject

SMFB guidelines

Register B

Pharmacist License

Pharmacy Council of Bangladesh

6 subjects

Core Content Areas

PCB syllabus

75%

Attendance Requirement

SMFB regulations

Written & Oral

Assessment Formats

SMFB Final Exam

The Bangladesh Diploma in Pharmacy Final Exam is administered by the State Medical Faculty (SMFB) in collaboration with the Pharmacy Council of Bangladesh (PCB). The curriculum is a 3-year diploma, and the final exam requires a 50% score in both written (theory) and practical/oral evaluations. Achieving this qualification allows registration as a Register B (B-Grade) pharmacist in Bangladesh, permitting retail practice, hospital dispensing, and pharmaceutical manufacturing technician roles.

Sample State Medical Faculty Diploma in Pharmacy Final Exam Practice Questions

Try these sample questions to test your State Medical Faculty Diploma in Pharmacy Final Exam exam readiness. Each question includes a detailed explanation. Start the interactive quiz above for the full 100+ question experience with AI tutoring.

1How much water must be added to 500 mL of 70% v/v alcohol to dilute it to a 40% v/v alcohol solution?
A.250 mL
B.375 mL
C.500 mL
D.875 mL
Explanation: Using the dilution equation V1 * C1 = V2 * C2, we have 500 mL * 70% = V2 * 40%, which gives a final total volume (V2) of 875 mL. The amount of water to be added is the final volume minus the initial volume: 875 mL - 500 mL = 375 mL.
2Under the British-derived system used in Bangladesh, what is the proof strength of a solution containing 50% v/v ethyl alcohol?
A.87.5° proof
B.12.5° under proof
C.12.5° over proof
D.50.0° proof
Explanation: In the British proof system, 100% v/v alcohol is equivalent to 175.25° proof (or 75.25° over proof). To find the proof strength of 50% v/v alcohol, multiply the volume percentage by 1.7525: 50 * 1.7525 = 87.625° proof. Since this is less than 100°, it is designated as under proof (100 - 87.625 = 12.375° under proof, which rounds closely to 12.5° under proof).
3Which of the following excipients is primarily used as a disintegrant in tablet formulations?
A.Magnesium stearate
B.Lactose
C.Starch
D.Ethylcellulose
Explanation: Starch is a widely used disintegrant because it absorbs moisture and swells rapidly in the gastrointestinal tract, causing the tablet to break apart. Magnesium stearate is a lubricant, lactose is a diluent/filler, and ethylcellulose is a water-insoluble coating polymer used for modified release.
4Which sterilization method is most appropriate for a heat-sensitive (thermolabile) ophthalmic solution containing a polypeptide drug?
A.Autoclaving at 121°C for 15 minutes
B.Dry heat sterilization at 170°C for 2 hours
C.Membrane filtration through a 0.22-micron filter
D.Exposure to ethylene oxide gas
Explanation: Heat-sensitive liquids will degrade under steam (autoclaving) or dry heat sterilization. Membrane filtration through a 0.22-micron filter physically removes microorganisms without applying heat, making it the standard method for sterilizing thermolabile liquid formulations. Ethylene oxide is used for moisture/heat-sensitive solid equipment, not liquid solutions.
5In the dye solubility test, when an oil-soluble dye like Scarlet Red is added to an emulsion and the droplets become colored while the background remains clear, what type of emulsion is it?
A.Oil-in-water (o/w) emulsion
B.Water-in-oil (w/o) emulsion
C.Multiple emulsion
D.Microemulsion
Explanation: In an oil-in-water (o/w) emulsion, oil is the dispersed phase (droplets) and water is the continuous phase. Adding an oil-soluble dye will selectively color the oil droplets, leaving the continuous water phase clear. If it were a w/o emulsion, the entire continuous oil background would become colored.
6What is the primary mechanism of action of bentonite when used as a suspending agent in pharmaceutical suspensions?
A.It reduces the interfacial tension between the liquid and solid phases
B.It increases the viscosity of the continuous phase and acts as a protective colloid
C.It acts as a chemical preservative to prevent fungal growth
D.It increases the solubility of the drug particles in water
Explanation: Bentonite is an inorganic clay that swells in water to form a thixotropic gel. It increases the viscosity of the continuous phase, which slows down the sedimentation rate of the suspended particles according to Stokes' law. It does not significantly reduce interfacial tension (which is the role of surfactants) or act as a preservative.
7According to Stokes' law of sedimentation, which of the following changes would decrease the rate of sedimentation of particles in a suspension?
A.Increasing the particle size of the dispersed phase
B.Increasing the viscosity of the continuous medium
C.Increasing the density difference between the particles and the medium
D.Increasing the acceleration due to gravity
Explanation: Stokes' law states that the sedimentation rate (v) is inversely proportional to the viscosity of the medium (n). Therefore, increasing the viscosity of the continuous phase will decrease the sedimentation rate. Increasing particle size, density difference, or gravity will all increase the sedimentation rate.
8Which of the following is a water-soluble base commonly used for the preparation of suppositories?
A.Cocoa butter (Theobroma oil)
B.Polyethylene glycol (Macrogol)
C.Hydrogenated vegetable oil
D.Emulsifying wax
Explanation: Polyethylene glycol (PEG), also known as macrogol, is a water-soluble synthetic polymer base that dissolves in the body's fluids rather than melting at body temperature. Cocoa butter and hydrogenated vegetable oils are oleaginous (fatty) bases that melt at body temperature.
9What is the primary function of a humectant, such as glycerin or propylene glycol, in a topical cream or ointment?
A.To provide a pleasant fragrance to the formulation
B.To prevent the loss of moisture and drying out of the preparation
C.To act as a primary emulsifying agent for o/w systems
D.To neutralize acidic impurities in the base
Explanation: Humectants are hygroscopic substances added to topical formulations (like creams) to retain water, preventing the product from drying out and crusting during storage and use. They also help keep the skin hydrated upon application. They do not act as emulsifiers or chemical neutralizers.
10Calculate the dose of a drug for a 6-year-old child if the adult dose is 500 mg, using Young's rule.
A.125 mg
B.166.7 mg
C.250 mg
D.333.3 mg
Explanation: Young's rule is: Child Dose = [Age / (Age + 12)] * Adult Dose. Applying this: Child Dose = [6 / (6 + 12)] * 500 mg = [6 / 18] * 500 mg = (1/3) * 500 mg = 166.67 mg.

About the State Medical Faculty Diploma in Pharmacy Final Exam Exam

The State Medical Faculty Diploma in Pharmacy Final Exam in Bangladesh is the concluding academic assessment for the 3-year Diploma in Pharmacy program. Passing this examination is a prerequisite for candidates to receive their Diploma certificate and subsequently apply to the Pharmacy Council of Bangladesh (PCB) for Register B (B-Grade) Pharmacist registration. The exam covers critical modules including Pharmaceutics, Pharmacology, Pharmaceutical Chemistry, Pharmacognosy, Forensic Pharmacy Laws, and Hospital/Clinical Pharmacy.

Assessment

Multiple-choice questions (MCQs), short answer questions, practical assignments, and oral viva voce.

Time Limit

3 hours (per written paper)

Passing Score

50% in theory and 50% in practical/oral components separately

Exam Fee

Varies by institute (State Medical Faculty of Bangladesh & Pharmacy Council of Bangladesh)

State Medical Faculty Diploma in Pharmacy Final Exam Exam Content Outline

25%

Pharmacology

General pharmacology principles, pharmacokinetics, pharmacodynamics, systemic drugs (cardiovascular, CNS, autonomic, antibiotics), and toxicity profiles.

20%

Pharmaceutics

Physical pharmacy, dispensing calculations, compounding, dosage forms (tablets, capsules, syrups, sterile preparations), and labeling requirements.

20%

Pharmaceutical Chemistry

Inorganic and organic pharmaceutical chemistry, biochemistry, structure-activity relationships, drug synthesis basics, and chemical assay techniques.

15%

Pharmacognosy

Study of crude drugs from plants and animal sources, phytochemical screening, therapeutic uses of medicinal plants, and extraction methods.

10%

Forensic Pharmacy Laws & Ethics

Bangladesh Pharmacy Act, Drugs Act 1940, Drug Control Ordinance 1982, Narcotic Drugs and Psychotropic Substances Act, and pharmacist code of conduct.

10%

Hospital & Clinical Pharmacy

Hospital pharmacy organization, formulary systems, unit-dose drug distribution, patient counseling, adverse reaction reporting, and clinical pharmacy basics.

How to Pass the State Medical Faculty Diploma in Pharmacy Final Exam Exam

What You Need to Know

  • Passing score: 50% in theory and 50% in practical/oral components separately
  • Assessment: Multiple-choice questions (MCQs), short answer questions, practical assignments, and oral viva voce.
  • Time limit: 3 hours (per written paper)
  • Exam fee: Varies by institute

Keys to Passing

  • Complete 500+ practice questions
  • Score 80%+ consistently before scheduling
  • Focus on highest-weighted sections
  • Use our AI tutor for tough concepts

State Medical Faculty Diploma in Pharmacy Final Exam Study Tips from Top Performers

1Master the drug acts and regulations, especially the Drugs Act 1940 and Drug Control Ordinance 1982, as they are tested heavily in Forensic Pharmacy.
2Understand the classification of crude drugs (alkaloids, glycosides, tannins, volatile oils) and botanical names of common medicinal plants in Bangladesh.
3Practice dispensing and pharmaceutical calculations, including dilution, dosage adjustments, and isotonicity calculations, which are crucial for the Pharmaceutics practical.
4Learn the mechanisms of action, major indications, and adverse effects of primary therapeutic classes (NSAIDs, antihypertensives, antidiabetics, and antimicrobials).
5Focus on the differences between hospital pharmacy and clinical pharmacy, including patient profiling, drug-drug interactions, and patient counseling steps.

Frequently Asked Questions

What is the State Medical Faculty Diploma in Pharmacy?

It is a 3-year professional diploma program in pharmacy regulated by the State Medical Faculty of Bangladesh (SMFB) in cooperation with the Pharmacy Council of Bangladesh (PCB). It provides standard vocational and technical training for prospective pharmacists.

How do I become a B-Grade Registered Pharmacist in Bangladesh?

You must complete the 3-year Diploma in Pharmacy from a recognized institute, pass the final examinations conducted by the State Medical Faculty of Bangladesh, and then submit your application for B-Grade registration to the Pharmacy Council of Bangladesh (PCB).

What are the passing criteria for the final exam?

Students must score at least 50% in the written theory examination and 50% in the practical/oral/viva voce examination separately for each subject. Failing in either the theory or practical section of a subject requires retaking that entire subject.

What subjects are included in the final examination?

The examination tests several core areas: Pharmaceutics, Pharmacology, Pharmaceutical Chemistry, Pharmacognosy, Forensic Pharmacy Laws, and Hospital/Clinical Pharmacy.

What is the fee for the examination?

The exam registration fee is decided by the State Medical Faculty for each batch. It typically ranges from 2,000 to 5,000 BDT depending on the exam center, registration timing, and institutional requirements. Check with your institute's registrar for the exact amount.

What career opportunities are available after passing?

Graduates can apply for B-Grade registration to own and operate retail pharmacy stores, work as pharmacy technicians or supervisors in hospital pharmacies, or work as quality control/production technicians in Bangladesh's pharmaceutical manufacturing industry.