Medical Laboratory Science
AHPC Licensure Examination — Medical Laboratory Science
Professional licensing examination for medical laboratory scientists in Ghana.
- Practice questions
- 204
- Flashcards
- 130
- Topics
- 18
- Mock exam
- 100 questions · 150 min · pass 60%
What the AHPC Licensure Examination — Medical Laboratory Science covers
Our questions are organised by subject and topic, following the exam syllabus.
Haematology & Transfusion Science
- Complete Blood Count & Blood Films 16 Qs · 10 cards
- Haemostasis & Coagulation 11 Qs · 7 cards
- Blood Groups, Compatibility & Transfusion Safety 12 Qs · 9 cards
Clinical Chemistry
- Renal, Liver & Cardiac Function Tests 12 Qs · 7 cards
- Glucose, Lipids & Endocrine Testing 12 Qs · 7 cards
- Analytical Methods & Instrumentation 11 Qs · 6 cards
Medical Microbiology
- Bacteriology & Antimicrobial Susceptibility 15 Qs · 8 cards
- Mycology & Virology 11 Qs · 7 cards
- Sterilisation, Disinfection & Biosafety 10 Qs · 6 cards
Parasitology & Immunology
- Malaria & Blood Parasites 12 Qs · 8 cards
- Intestinal & Tissue Parasites 11 Qs · 8 cards
- Serology, Immunology & Molecular Diagnostics 10 Qs · 7 cards
Histopathology & Cytology
- Specimen Fixation & Tissue Processing 10 Qs · 7 cards
- Histological Stains & Microscopy 10 Qs · 7 cards
- Cytology & Cellular Pathology 9 Qs · 7 cards
Laboratory Quality & Professional Practice
- Pre-analytical, Analytical & Post-analytical Quality 9 Qs · 5 cards
- Internal Quality Control & External Assessment 10 Qs · 7 cards
- Laboratory Safety, Ethics & Information Management 13 Qs · 7 cards
Sample Medical Laboratory Science practice questions
Try these 12 questions from different topics. Open "Show answer" to check yourself and read the explanation.
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Question 1 · Complete Blood Count & Blood Films
An automated complete blood count is flagged for an abnormal cell population. What is the most appropriate next laboratory step?
- A.Review a well-prepared peripheral blood film according to procedure
- B.Delete the analyzer flag
- C.Report a normal differential without review
- D.Replace the patient result with the control value
Show answer
Answer: A. Review a well-prepared peripheral blood film according to procedure
Blood-film review can verify counts and assess cell morphology when analyzer flags or clinical findings require it.
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Question 2 · Haemostasis & Coagulation
A citrate tube submitted for coagulation testing is visibly clotted. What should the laboratory do?
- A.Remove the clot and continue testing
- B.Reject the specimen and request recollection according to policy
- C.Add extra anticoagulant after collection
- D.Report a result estimated from another patient
Show answer
Answer: B. Reject the specimen and request recollection according to policy
A clotted coagulation specimen no longer has a valid blood-to-anticoagulant relationship and can produce unreliable results.
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Question 3 · Blood Groups, Compatibility & Transfusion Safety
Agglutination is observed when a patient's serum is cross-matched with donor red cells. How should the unit be interpreted?
- A.Compatible because agglutination is expected
- B.Automatically group O
- C.Incompatible and not suitable for that patient
- D.Suitable if transfused slowly
Show answer
Answer: C. Incompatible and not suitable for that patient
Agglutination or haemolysis in the cross-match indicates incompatibility and the unit must not be issued for that patient.
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Question 4 · Renal, Liver & Cardiac Function Tests
A serum specimen is markedly haemolysed. What should happen before reporting chemistry results that may be affected?
- A.Ignore the specimen condition
- B.Change all results into the reference interval
- C.Report results without documenting haemolysis
- D.Assess the interference and follow the laboratory's rejection or comment policy
Show answer
Answer: D. Assess the interference and follow the laboratory's rejection or comment policy
Specimen integrity is part of pre-analytical quality; haemolysis may bias several analytes and must be managed consistently.
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Question 5 · Glucose, Lipids & Endocrine Testing
Internal quality control for a glucose assay is outside the acceptable range. What should the laboratory do?
- A.Do not release affected patient results until the problem is resolved
- B.Release results and investigate next month
- C.Adjust patient values to match the reference interval
- D.Delete the control result
Show answer
Answer: A. Do not release affected patient results until the problem is resolved
An unacceptable control result means the analytical run may be unreliable and requires investigation before release.
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Question 6 · Analytical Methods & Instrumentation
Which statement best distinguishes calibration from internal quality control?
- A.They are identical processes
- B.Calibration establishes the measurement relationship; control material monitors ongoing performance
- C.Calibration replaces all control testing
- D.Quality control is performed only when an instrument breaks
Show answer
Answer: B. Calibration establishes the measurement relationship; control material monitors ongoing performance
Calibration sets the analytical response, while routine controls help detect drift, imprecision or other performance problems.
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Question 7 · Bacteriology & Antimicrobial Susceptibility
Why must inoculum preparation be standardized for antimicrobial susceptibility testing?
- A.It changes the patient's identity
- B.It makes quality-control strains unnecessary
- C.Inoculum density affects inhibition zones or MIC results and therefore interpretation
- D.It guarantees every organism is susceptible
Show answer
Answer: C. Inoculum density affects inhibition zones or MIC results and therefore interpretation
Standardized inoculum and controlled methods are essential for reproducible, clinically useful susceptibility results.
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Question 8 · Mycology & Virology
A respiratory virus is suspected. Which method is generally more appropriate than routine culture on ordinary bacteriological agar?
- A.A routine Gram stain alone
- B.An oxidase test alone
- C.A bacterial disk-diffusion plate
- D.A validated viral nucleic-acid or antigen detection assay
Show answer
Answer: D. A validated viral nucleic-acid or antigen detection assay
Viruses require specialized detection systems; validated molecular or antigen methods are commonly used for diagnosis.
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Question 9 · Sterilisation, Disinfection & Biosafety
Before introducing a new laboratory procedure, what is the first biosafety planning step?
- A.Perform a risk assessment for the hazards and planned controls
- B.Assume every procedure has the same risk
- C.Wait for an exposure before selecting controls
- D.Use personal protective equipment as the only possible control
Show answer
Answer: A. Perform a risk assessment for the hazards and planned controls
Risk assessment identifies hazards, likelihood and consequences so layered controls can be selected appropriately.
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Question 10 · Malaria & Blood Parasites
Which blood film is most useful for sensitive screening for malaria parasites?
- A.An unstained urine sediment
- B.A properly prepared thick blood film
- C.A bacterial Gram-stain plate
- D.A cervical cytology smear
Show answer
Answer: B. A properly prepared thick blood film
Lysis of red cells concentrates parasites in a thick film, making it useful for screening; thin films support species identification.
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Question 11 · Intestinal & Tissue Parasites
Why may repeated stool examinations or concentration methods be needed when intestinal parasitic infection is suspected?
- A.Parasites are never visible microscopically
- B.Every preserved sample is unsuitable
- C.Eggs, cysts or oocysts may be passed intermittently or in small numbers
- D.One negative result proves every parasite is absent
Show answer
Answer: C. Eggs, cysts or oocysts may be passed intermittently or in small numbers
Intermittent or low-level shedding can reduce sensitivity, so repeat or concentrated examination may improve detection.
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Question 12 · Serology, Immunology & Molecular Diagnostics
A PCR run has no amplification in its positive control. How should patient results from that run be handled?
- A.Report every patient as negative
- B.Ignore the control because patients amplified differently
- C.Change the positive control result manually
- D.Treat the run as invalid and investigate before reporting
Show answer
Answer: D. Treat the run as invalid and investigate before reporting
A failed positive control means the run did not demonstrate that the assay could detect its target, so negative patient results are not valid.
Sample flashcards
Quick facts to revise. Members can study every card with Learn, Test and Match modes.
- Anticoagulant for FBC
- EDTA — preserves cell morphology by chelating calcium
- Coagulation tube ratio
- 9 parts blood : 1 part 3.2% sodium citrate — fill to the line
- Group O plasma
- Anti-A and anti-B; group AB has neither
- GFR marker in routine use
- Serum creatinine (eGFR equations)
- Glucose sample preservative
- Sodium fluoride (inhibits glycolysis) + oxalate
- Beer–Lambert law
- A = εcl — absorbance ∝ concentration × path length
- Gram stain critical step
- Decolourisation (acetone-alcohol)
- Fungal culture medium
- Sabouraud dextrose agar
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