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Medical Laboratory Technologist Prometric exam questions with answers

15 original practice questions written to the Medical Laboratory Technologist exam blueprint, each with the answer and why the other options are wrong. Below them: the Medical Laboratory Technologist exam's format, pass mark and fee at DHA, DOH, SCFHS, QCHP and every other GCC regulator, from their own published rules.

15
Free questions
50%
DHA pass mark
150
Questions on the DHA exam
25
Questions in the free mock

Quick answer

The Medical Laboratory Technologist exam is 150 MCQs in 3 hours at DHA (pass mark 50%), 200 MCQs in 240 minutes at SCFHS (pass mark 554 on a 200-800 scale) and 150 MCQs in 3 hours at QCHP (pass mark 50%). Below are 15 original practice questions written to the official blueprint, each with the answer and why the other options are wrong, plus a free 25-question timed mock.

The Medical Laboratory Technologist exam in every GCC country

DHA, SCFHS, QCHP publish an exact Medical Laboratory Technologist exam; the others apply one format to every title. Figures come from each regulator's own exam pages - anything not published says so.

Medical Laboratory Technologist licensing exam in every GCC country
RegulatorExamFormatPass markFee per attemptPractise
DHA
Dubai
Medical Laboratory Technologist (LAB5631)150 MCQs in 3 hours50%USD 240 (about AED 880)DHA questions →
DOH
Abu Dhabi, Al Ain and Al Dhafra
DOH licensing exam
Regulator-wide format
Written + oral/OSCEPass / fail onlyNot publishedDOH questions →
MOHAP
Northern Emirates - Ajman, Umm Al Quwain, Ras Al Khaimah and Fujairah
MOHAP licensing exam
Regulator-wide format
Computer-basedNot publishedNot publishedMOHAP questions →
SHA
Emirate of Sharjah
SHA licensing exam
Regulator-wide format
Set at assessmentNot publishedNot publishedSHA questions →
SCFHS
Kingdom of Saudi Arabia
Saudi Laboratory Specialist Licensure Examination (SLLE)200 MCQs in 240 minutes554 on a 200-800 scaleNot publishedSCFHS questions →
QCHP
State of Qatar
Lab Technologist150 MCQs in 3 hours50%Not publishedQCHP questions →
NHRA
Kingdom of Bahrain
NHRA licensing exam
Regulator-wide format
Prometric CBTNot publishedNot publishedNHRA questions →
OMSB
Sultanate of Oman
OMSB licensing exam
Regulator-wide format
Computer-based OC examNot publishedNot publishedOMSB questions →
Kuwait MOH
State of Kuwait
Kuwait MOH licensing exam
Regulator-wide format
150 MCQs, 170 min60-70%Not publishedKuwait MOH questions →

exact exam published for Medical Laboratory Technologist

Pass marks, attempts and fees change - confirm yours on the regulator's exam page before you book.

15 Medical Laboratory Technologist exam questions with answers

Choose your answer first, then open the explanation. The set covers the main blueprint domains at a mix of easy, medium and hard.

  1. Question 1General Laboratory, Quality Management & Safetymedium

    On a chemistry analyser, the same level of control material gives values above +2 SD on two consecutive runs, while the other level is within limits. Which interpretation and action are correct under Westgard rules?

    1. AA 1-2s warning only; accept the run and continue testing
    2. BA 2-2s violation (systematic error); reject the run and investigate
    3. CAn R-4s violation suggesting random error; repeat one control
    4. DA 10x violation; no action until ten results are available
    Show answer and explanation

    Answer: B. A 2-2s violation (systematic error); reject the run and investigate

    Two consecutive control values exceeding the same 2 SD limit is a 2-2s rule violation, which points to systematic error such as calibration drift or reagent deterioration, so patient results are held and the cause is investigated. A 1-2s result is only a warning when a single value is outside 2 SD, which does not apply when the rule has already been broken on consecutive runs.

  2. Question 2Clinical Chemistryeasy

    A blood sample arrives visibly haemolysed after a difficult venepuncture. Which analyte is most likely to be falsely increased?

    1. ASodium
    2. BGlucose
    3. CAlbumin
    4. DPotassium
    Show answer and explanation

    Answer: D. Potassium

    Red cells contain far more potassium than plasma, so in vitro haemolysis releases potassium and falsely raises the result; LDH, AST and phosphate are also increased. Sodium is mainly extracellular and is not significantly raised by haemolysis, and glucose is more affected by delayed separation than by haemolysis.

  3. Question 3Clinical Chemistrymedium

    A patient with suspected ketoacidosis has sodium 140 mmol/L, potassium 4.5 mmol/L, chloride 100 mmol/L and bicarbonate 10 mmol/L. Using the formula that excludes potassium, what is the anion gap?

    1. A30 mmol/L
    2. B10 mmol/L
    3. C50 mmol/L
    4. D20 mmol/L
    Show answer and explanation

    Answer: A. 30 mmol/L

    Anion gap = Na - (Cl + HCO3) = 140 - (100 + 10) = 30 mmol/L, which is raised and consistent with a high anion gap metabolic acidosis such as ketoacidosis. A result of 50 mmol/L comes from adding bicarbonate instead of subtracting it, and the usual reference range without potassium is roughly 8-16 mmol/L.

  4. Question 4Clinical Chemistryhard

    An outpatient who is clinically well with a normal ECG has serum potassium 9.6 mmol/L, calcium 0.6 mmol/L (2.4 mg/dL) and a very low alkaline phosphatase. The sample is not haemolysed. What is the most likely explanation?

    1. AAcute kidney injury with severe hyperkalaemia
    2. BPrimary hypoparathyroidism with renal tubular acidosis
    3. CContamination of the serum sample with K2EDTA anticoagulant
    4. DPseudohyperkalaemia caused by a high platelet count
    Show answer and explanation

    Answer: C. Contamination of the serum sample with K2EDTA anticoagulant

    K2EDTA contamination, for example from an incorrect order of draw or decanting, adds potassium and chelates calcium, magnesium and zinc, giving spurious hyperkalaemia, profound hypocalcaemia and low ALP (a zinc and magnesium dependent enzyme) in a well patient; the sample should be recollected. True hyperkalaemia at this level would almost always produce ECG changes, and thrombocytosis does not explain the hypocalcaemia.

  5. Question 5Hematologymedium

    A 35-year-old woman has fever, confusion, anaemia, a platelet count of 18 x 10^9/L, raised LDH and impaired renal function. Coagulation screen is normal. Which blood film finding most supports thrombotic thrombocytopenic purpura?

    1. ASpherocytes (dense round red cells)
    2. BTarget cells (codocytes)
    3. CSchistocytes (fragmented red cells)
    4. DBite cells (degmacytes)
    Show answer and explanation

    Answer: C. Schistocytes (fragmented red cells)

    TTP is a thrombotic microangiopathy, in which red cells are sheared by microthrombi, producing schistocytes with thrombocytopenia and haemolysis; a normal coagulation screen helps distinguish it from DIC. Spherocytes are typical of hereditary spherocytosis and warm autoimmune haemolysis, and bite cells suggest oxidative haemolysis such as G6PD deficiency.

  6. Question 6Hematologyhard

    A child with intermittent jaundice and splenomegaly has a raised MCHC, numerous spherocytes on the film, a negative direct antiglobulin test and a family history of similar problems. Which test is preferred to confirm the likely diagnosis?

    1. AEosin-5-maleimide (EMA) binding test
    2. BHaemoglobin electrophoresis by HPLC
    3. CQuantitative G6PD enzyme assay
    4. DHam acid serum lysis test
    Show answer and explanation

    Answer: A. Eosin-5-maleimide (EMA) binding test

    Spherocytes with a raised MCHC, a negative DAT and a positive family history suggest hereditary spherocytosis, and the EMA binding test, which detects reduced band 3 on the red cell membrane, is the recommended screening and confirmation test. The negative DAT excludes autoimmune haemolysis, while haemoglobin electrophoresis assesses haemoglobinopathies rather than membrane defects.

  7. Question 7Hematologyeasy

    Needle-shaped azurophilic inclusions are seen in the cytoplasm of blasts on a bone marrow aspirate. These Auer rods indicate which condition?

    1. AAcute lymphoblastic leukaemia
    2. BChronic lymphocytic leukaemia
    3. CChronic myeloid leukaemia in chronic phase
    4. DAcute myeloid leukaemia
    Show answer and explanation

    Answer: D. Acute myeloid leukaemia

    Auer rods are fused primary (azurophilic) granules and are found in myeloid blasts, so they confirm a myeloid lineage and are characteristic of AML, particularly acute promyelocytic leukaemia. Lymphoblasts in ALL do not contain Auer rods, which is why they are a useful morphological discriminator.

  8. Question 8Coagulation & Hemostasismedium

    A patient who takes no medication has a prolonged prothrombin time with a normal activated partial thromboplastin time. Deficiency of which single factor best explains this pattern?

    1. AFactor VIII
    2. BFactor VII
    3. CFactor IX
    4. DFactor XII
    Show answer and explanation

    Answer: B. Factor VII

    Factor VII is the only factor unique to the extrinsic pathway measured by the PT, so its deficiency prolongs the PT alone. Deficiencies of factors VIII, IX and XII affect the intrinsic pathway and prolong the aPTT with a normal PT.

Halfway - how are you scoring?

Test yourself under real exam conditions

The free 25-question mock is timed and scored against the pass mark, domain by domain, so you see exactly where you are losing marks. The full Medical Laboratory Technologist bank has 3 full-length papers (about 444 questions) for AED 249, one-time.

  1. Question 9Coagulation & Hemostasishard

    A coagulation sample is requested on a patient with polycythaemia whose haematocrit is 65%. What adjustment is needed to avoid falsely prolonged clotting times?

    1. AReduce the volume of sodium citrate in the tube before collection
    2. BIncrease the volume of sodium citrate in the tube before collection
    3. CCollect the sample into a lithium heparin tube instead
    4. DUnderfill the standard citrate tube to about half its volume
    Show answer and explanation

    Answer: A. Reduce the volume of sodium citrate in the tube before collection

    With a very high haematocrit, the plasma volume is small, so the standard citrate volume is excessive relative to plasma, causing over-anticoagulation and falsely prolonged PT and aPTT; CLSI guidance is to reduce citrate volume when the haematocrit exceeds 55%. Adding more citrate or underfilling the tube would worsen the citrate-to-plasma excess.

  2. Question 10Immunology & Serologymedium

    A healthcare worker's hepatitis B serology shows HBsAg negative, total anti-HBc positive and anti-HBs positive. How should this be interpreted?

    1. AImmunity from hepatitis B vaccination only, with no past infection
    2. BChronic hepatitis B infection with ongoing viral replication
    3. CPast hepatitis B infection that has resolved, with natural immunity
    4. DAcute hepatitis B infection in the window period
    Show answer and explanation

    Answer: C. Past hepatitis B infection that has resolved, with natural immunity

    Anti-HBc is produced only after natural infection, and anti-HBs with a negative HBsAg indicates clearance and immunity, so the pattern represents resolved past infection. Vaccination produces anti-HBs alone without anti-HBc, which is the most common source of confusion. Chronic infection would show a positive HBsAg.

  3. Question 11Immunohematology (Blood Group Serology)hard

    Ten days after a red cell transfusion, a patient develops falling haemoglobin, mild jaundice and a newly positive DAT. The pre-transfusion antibody screen was negative. Which antibody is classically implicated in this type of reaction?

    1. AAnti-Lea
    2. BAnti-Jka
    3. CAnti-M
    4. DAnti-P1
    Show answer and explanation

    Answer: B. Anti-Jka

    Kidd antibodies such as anti-Jka are notorious for causing delayed haemolytic transfusion reactions because they often fall to undetectable levels and then rise rapidly on re-exposure (an anamnestic response); they also show dosage. Lewis, M and P1 antibodies are usually IgM, cold-reactive and rarely clinically significant, so they are unlikely causes.

  4. Question 12Blood Banking & Transfusion Serviceseasy

    A trauma patient of unknown blood group needs plasma urgently. Which ABO group of plasma can be given safely before the patient's group is known?

    1. AGroup O
    2. BGroup A
    3. CGroup B
    4. DGroup AB
    Show answer and explanation

    Answer: D. Group AB

    Group AB plasma contains neither anti-A nor anti-B, so it is compatible with recipients of any ABO group and is the universal plasma donor group. Group O is the universal donor for red cells, but group O plasma contains both anti-A and anti-B and can haemolyse non-O red cells.

  5. Question 13Blood Banking & Transfusion Servicesmedium

    How should platelet concentrates be stored to maintain their function until transfusion?

    1. AAt 2-6 C in a monitored blood bank refrigerator
    2. BAt 20-24 C without agitation to avoid activation
    3. CAt -18 C or colder in a plasma freezer
    4. DAt 20-24 C with continuous gentle agitation
    Show answer and explanation

    Answer: D. At 20-24 C with continuous gentle agitation

    Platelets are stored at room temperature (20-24 C) with continuous agitation to maintain gas exchange and pH and preserve function, usually for 5-7 days depending on the system. Refrigeration causes cold-induced clearance of standard platelets, and storing without agitation leads to a fall in pH and loss of viability. Room-temperature storage also makes bacterial contamination the main infective risk.

  6. Question 14Microbiologymedium

    A wound swab grows a non-lactose fermenting Gram-negative rod on MacConkey agar. It is oxidase positive, produces a blue-green pigment and has a grape-like odour. Which organism is most likely?

    1. APseudomonas aeruginosa
    2. BEscherichia coli
    3. CKlebsiella pneumoniae
    4. DProteus mirabilis
    Show answer and explanation

    Answer: A. Pseudomonas aeruginosa

    Pseudomonas aeruginosa is an oxidase-positive non-fermenter that produces pyocyanin (blue-green pigment) and a characteristic grape-like odour. Proteus mirabilis is also a non-lactose fermenter but is oxidase negative and swarms on blood agar, while E. coli and Klebsiella are lactose fermenters.

  7. Question 15Urinalysis & Body Fluidseasy

    A urine reagent strip shows a positive nitrite pad. What does this most likely indicate?

    1. AInfection with Enterococcus faecalis
    2. BBacteriuria with nitrate-reducing organisms such as E. coli
    3. CCandida infection of the urinary tract
    4. DContamination of the sample with vaginal epithelial cells
    Show answer and explanation

    Answer: B. Bacteriuria with nitrate-reducing organisms such as E. coli

    Many Gram-negative Enterobacterales, such as E. coli, reduce dietary nitrate to nitrite, so a positive nitrite test indicates significant bacteriuria. Enterococci and yeasts do not reduce nitrate, so a negative nitrite does not exclude infection with these organisms.

What the Medical Laboratory Technologist exam covers

The blueprint groups questions into these domains. Weight your revision the same way - the heavier domains carry more of your score.

General Laboratory, Quality Management & Safety

~20%

Laboratory quality management systems and total quality management · Quality control · Accuracy, precision, mean, standard deviation, coefficient of variation (CV)

Clinical Chemistry

~18%

Spectrophotometry, Beer-Lambert law, and photometric principles · Instrumentation · Carbohydrate metabolism

Hematology

~15%

Hematopoiesis and normal blood cell physiology and maturation · Complete blood count (CBC) parameters and RBC indices (MCV, MCH, MCHC, RDW) · Manual and automated counting of RBC, WBC, and platelets; hemocytometer use

Coagulation & Hemostasis

~5%

Primary and secondary hemostasis and the coagulation cascade (intrinsic, extrinsic, common pathways) · Prothrombin time (PT/INR) and clinical use in warfarin monitoring · Activated partial thromboplastin time (aPTT) and heparin monitoring

Immunology & Serology

~4%

Innate and adaptive immunity; cells and organs of the immune system · Antigen-antibody reactions, antibody structure, and the five immunoglobulin classes · Complement system and cytokines

Immunohematology (Blood Group Serology)

~10%

ABO blood group system · Rh blood group system · Other blood group systems

Blood Banking & Transfusion Services

~8%

Blood donor eligibility, screening, and deferral criteria · Blood collection, apheresis, and autologous/directed donation · Blood component preparation

Microbiology

~13%

Bacterial cell structure, morphology, and metabolism · Gram stain and other stains (acid-fast/Ziehl-Neelsen, KOH, India ink, spore) · Culture media types

Urinalysis & Body Fluids

~7%

Renal anatomy, urine formation, and physiology of the urinary system · Physical examination of urine · Chemical examination (dipstick)

How to answer these questions

1

Questions test applied practice: what you would do with this patient, this result or this image - not textbook definitions.

2

Safety items (radiation, infection control, patient identification, equipment checks) are high-yield and quick to revise.

3

Under time pressure, flag and move on: every question carries the same mark.

4

Aim to score comfortably above your regulator's pass mark - 10 to 15 points of margin - on timed, full-length practice before you book.

Medical Laboratory Technologist exam questions: FAQs

How many questions are in the Medical Laboratory Technologist Prometric exam?
It depends on the regulator: DHA 150 MCQs in 3 hours; SCFHS 200 MCQs in 240 minutes; QCHP 150 MCQs in 3 hours. The full table above lists every GCC regulator.
What is the pass mark for the Medical Laboratory Technologist exam?
DHA: 50%; SCFHS: 554 on a 200-800 scale; QCHP: 50%. Pass marks are set exam by exam, so use your own regulator's figure.
Are these real exam questions?
No. Regulators do not release their papers, and anything sold as a leaked paper is unofficial and risky to rely on. These are original questions written to the official exam blueprint, at the level and in the style of the real exam, each with a worked explanation.
Is the Medical Laboratory Technologist exam the same in every GCC country?
The clinical content is broadly similar because the exams test the same safe practice, but the format, length, pass mark, attempts and fees differ by regulator. Prepare on the content once, then check your regulator's exact rules before you book.
How should I use these questions?
Answer each one before opening the explanation, and note why each wrong option is wrong. Then take the free 25-question timed mock to see your score against the pass mark, and move to full-length papers when you score comfortably above it.

Last reviewed September 2026. Questions are original and written to the published exam blueprint; they are not taken from any real paper.

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