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Medical Laboratory Technologist Prometric exam questions

Chemistry, haematology, microbiology, blood bank and QC.

Tell us which regulator you are sitting and we send the bank prepared for that authority's exam.

For DHA · DOH · MOHAP · SHA · SCFHS · QCHP · NHRA · OMSB · Kuwait MOHDHA LAB5631OMSB OEMLSPass mark DHA 50% · QCHP 50% · OMSB 55% · Kuwait MOH 60%From 3 papers · ~150 Qs each
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What is riding on this exam

~AED 880
DHA exam fee, per attempt
Paid again on every re-sit. Other regulators' fees are in the table below.
3
UAE attempts - in total
Shared across DHA, DOH, MOHAP and SHA, not three each. Saudi, Qatar, Oman and Kuwait rules are in the FAQ.
50-60%
Pass mark, by regulator
DHA 50%, QCHP 50%, OMSB 55%, Kuwait MOH 60%. Other regulators in the table below.

One failed attempt costs you the fee again, plus months of delay on your licence, your visa and your start date. This bank costs about a third of one exam fee.

Every regulator: format, pass marks and fees for all GCC licensing exams, each from the regulator's own documents.

The Medical Laboratory Technologist exam at a glance

DHA (UAE) publishes a Medical Laboratory Technologist exam of 150 MCQs in 3 hours with a 50% pass mark; DOH (UAE) publishes a Medical Laboratory Technologist exam of 50-100 MCQs in 1-2 hours, scored pass or fail; SCFHS (Saudi Arabia) publishes a Medical Laboratory Technologist exam of 200 MCQs in 240 minutes with a 530 on a 200-800 scale pass mark; QCHP (Qatar) publishes a Medical Laboratory Technologist exam of 150 MCQs in 3 hours with a 50% pass mark; OMSB (Oman) publishes a Medical Laboratory Technologist exam of 100 MCQs in 150 minutes with a 55% pass mark; Kuwait MOH (Kuwait) publishes a Medical Laboratory Technologist exam of 150 MCQs in 170 minutes with a 60% pass mark. MOHAP, SHA, NHRA do not publish Medical Laboratory Technologist-specific figures; their regulator-wide format and pass-mark rules are in the full table.

DHA · UAE
Medical Laboratory Technologist (LAB5631)
150 MCQs in 3 hours · pass mark 50% · USD 240 (about AED 880) · checked September 2026
DOH · UAE
Medical Laboratory Technologist CBT
50-100 MCQs in 1-2 hours · pass mark Pass / fail only · AED 500 · checked October 2026
SCFHS · Saudi Arabia
Saudi Laboratory Specialist Licensure Examination (SLLE)
200 MCQs in 240 minutes · pass mark 530 on a 200-800 scale · checked October 2026
QCHP · Qatar
Lab Technologist
150 MCQs in 3 hours · pass mark 50% · checked September 2026
OMSB · Oman
Omani Examination for Medical Laboratory Specialists (OEMLS)
100 MCQs in 150 minutes · pass mark 55% · USD 200 (about OMR 80) · checked September 2026
Kuwait MOH · Kuwait
Lab Technician
150 MCQs in 170 minutes · pass mark 60% · checked September 2026

From each regulator's own exam documents; the DHA row is from the DHA CBT Guideline, Sep 2026. Every other regulator is in the full GCC table.

Try two questions from this bank

Original questions from the bank - pick an answer to see the rationale and reference.

Q1Microbiology

A beta-hemolytic Streptococcus from a throat swab is bacitracin-susceptible and PYR-positive. This organism is most likely which Lancefield group and species?

Choose an answer to see the rationale.

Q2Urinalysis & Body Fluids

A patient is instructed to prepare for a guaiac-based fecal occult blood test (gFOBT). Which dietary or medication factor is most likely to cause a FALSE-POSITIVE result?

Choose an answer to see the rationale.

Not sure where you stand? Sit 25 of these questions free, timed at real exam pace, and see which domains you are weakest in.

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What's inside

  • ✓3 to 6 full-length papers (~150 Q each)
  • ✓No question repeated between papers
  • ✓Four options, one unambiguous best answer
  • ✓A full rationale on every question
  • ✓A real guideline or textbook reference
  • ✓Every sub-topic in the published blueprint
  • ✓Researched by Neelim's exam research team
  • ✓Prepared for your authority's exam, not a generic set

The Medical Laboratory Technologist exam in every GCC country

Medical Laboratory Technologist licensing exam in every GCC country
RegulatorExamFormatPass markFee per attempt
Medical Laboratory Technologist (LAB5631)
150 MCQs in 3 hours50%USD 240 (about AED 880)
DOH
Abu Dhabi, Al Ain and Al Dhafra
Practise →
Medical Laboratory Technologist CBT
50-100 MCQs in 1-2 hoursPass / fail onlyAED 500
SCFHS
Kingdom of Saudi Arabia
Practise →
Saudi Laboratory Specialist Licensure Examination (SLLE)
200 MCQs in 240 minutes530 on a 200-800 scaleNot published
QCHP
State of Qatar
Practise →
Lab Technologist
150 MCQs in 3 hours50%Not published
OMSB
Sultanate of Oman
Practise →
Omani Examination for Medical Laboratory Specialists (OEMLS)
100 MCQs in 150 minutes55%USD 200 (about OMR 80)
Kuwait MOH
State of Kuwait
Practise →
Lab Technician
150 MCQs in 170 minutes60%Not published
MOHAP
Northern Emirates - Ajman, Umm Al Quwain, Ras Al Khaimah and Fujairah
Practise →
MOHAP licensing exam
Regulator-wide format
Computer-basedNot publishedNot published
SHA
Emirate of Sharjah
Practise →
SHA licensing exam
Regulator-wide format
Set at assessmentNot publishedNot published
NHRA
Kingdom of Bahrain
Practise →
NHRA licensing exam
Regulator-wide format
Prometric CBTNot publishedNot published

Highlighted rows publish figures for this exact Medical Laboratory Technologist exam; the others show the regulator's general rules.

From each regulator's own exam pages; anything a regulator does not publish says so. Assessment mode also depends on your licence title, so confirm your route on your eligibility notice.

Try 15 free Medical Laboratory Technologist questions with answersDifferent from the samples on this page - each with a full explanationStart →

What the Medical Laboratory Technologist exam covers

The published blueprint for this exam breaks into 9 domains and 147 testable sub-topics. Our bank covers every one of them - here is the full map, so you can see exactly what you are expected to know.

General Laboratory, Quality Management & Safety~20% (est.)20 topics
  • Laboratory quality management systems and total quality management
  • Quality control: Levey-Jennings charts, Westgard multirules (1-2s, 1-3s, 2-2s, R-4s, 4-1s, 10x)
  • Accuracy, precision, mean, standard deviation, coefficient of variation (CV)
  • Calibration, verification, and analytical measurement range
  • Sensitivity, specificity, predictive values, reference intervals and critical values
  • Internal QC vs external quality assessment / proficiency testing
  • +14 more in the bank
Clinical Chemistry~18% (est.)18 topics
  • Spectrophotometry, Beer-Lambert law, and photometric principles
  • Instrumentation: nephelometry, osmometry, blood gas analyzers, electrophoresis, immunoassay, ISE, chromatography
  • Carbohydrate metabolism: glucose testing, glucose tolerance test, HbA1c, and classification of diabetes mellitus
  • Renal function tests: urea/BUN, creatinine, eGFR, uric acid, and correlation with renal disease
  • Hepatic function tests: bilirubin (direct/indirect), ALT, AST, ALP, GGT, ammonia, and jaundice patterns
  • Enzymology: CK and isoenzymes, LD, amylase, lipase, ACP, clinical significance and tissue sources
  • +12 more in the bank
Hematology~15% (est.)18 topics
  • 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
  • Hemoglobin and hematocrit determination and sources of error
  • Peripheral blood smear preparation, staining (Wright/Giemsa), and RBC morphology
  • Anemia classification: microcytic, normocytic, macrocytic and underlying causes
  • +12 more in the bank
Coagulation & Hemostasis~5% (est.)12 topics
  • 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
  • Fibrinogen assay and thrombin time
  • D-dimer, fibrin degradation products (FDP/FSP), and DIC evaluation
  • Mixing studies to distinguish factor deficiency from inhibitors
  • +6 more in the bank
Immunology & Serology~4% (est.)15 topics
  • 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
  • Hypersensitivity reactions (types I-IV) and autoimmunity
  • Serologic methods: agglutination, precipitation, ELISA, immunofluorescence, Western blot
  • Nephelometry and turbidimetry for serum proteins
  • +9 more in the bank
Immunohematology (Blood Group Serology)~10% (est.)16 topics
  • ABO blood group system: genetics, H/A/B antigens, forward and reverse typing
  • Rh blood group system: D antigen, weak D (Du) testing, and Rh phenotypes
  • Other blood group systems: MNS, Duffy, Kidd, Lewis, Kell, P
  • Antibody screening and identification using panel cells
  • Naturally occurring vs immune antibodies; warm and cold reacting antibodies
  • Direct antiglobulin test (DAT) and indirect antiglobulin test (IAT) principles
  • +10 more in the bank
Blood Banking & Transfusion Services~8% (est.)14 topics
  • Blood donor eligibility, screening, and deferral criteria
  • Blood collection, apheresis, and autologous/directed donation
  • Blood component preparation: red cells, platelets, FFP, cryoprecipitate
  • Component storage temperatures, shelf life, and quality requirements
  • Transfusion-transmitted infection screening (HBV, HCV, HIV, syphilis, HTLV, malaria)
  • Acute and delayed hemolytic transfusion reactions
  • +8 more in the bank
Microbiology~13% (est.)18 topics
  • Bacterial cell structure, morphology, and metabolism
  • Gram stain and other stains (acid-fast/Ziehl-Neelsen, KOH, India ink, spore)
  • Culture media types: enriched, selective, differential, and their QC
  • Specimen collection, transport, and acceptability criteria by site
  • Gram-positive cocci: Staphylococcus and Streptococcus identification
  • Gram-negative rods: Enterobacteriaceae, Pseudomonas, and identification schemes
  • +12 more in the bank
Urinalysis & Body Fluids~7% (est.)16 topics
  • Renal anatomy, urine formation, and physiology of the urinary system
  • Physical examination of urine: color, clarity, and specific gravity
  • Chemical examination (dipstick): pH, protein, glucose, ketones, blood, bilirubin, urobilinogen, nitrite, leukocyte esterase
  • Reagent strip principles, sources of error, and interferences
  • Confirmatory tests: sulfosalicylic acid (protein), Ictotest (bilirubin), Clinitest/Acetest
  • Microscopic examination: RBCs, WBCs, epithelial cells
  • +10 more in the bank

12 worked Medical Laboratory Technologist practice questions

Original exam-style questions from the bank, spread across the blueprint domains. They are not real or recalled exam questions. Try each one, then open the answer for the rationale and reference. None of them appear in the free mock exam, so reading them will not spoil it.

  1. Question 1 · General Laboratory, Quality Management & Safety

    A healthcare worker with a documented adequate anti-HBs antibody response (a known responder) sustains a needlestick from a hepatitis B surface antigen-positive source. What is the recommended post-exposure management for hepatitis B?

    1. AAdminister hepatitis B immune globulin (HBIG) plus a full new vaccine series
    2. BRestart the vaccine series only, without HBIG
    3. CAdminister two doses of HBIG one month apart
    4. DNo hepatitis B treatment is needed because the worker is an immune responder
    Show answer and explanation

    Correct answer: D. No hepatitis B treatment is needed because the worker is an immune responder

    A vaccinated worker with a documented adequate anti-HBs level (>=10 mIU/mL, a known responder) is considered protected and needs no HBIG or additional vaccine after HBsAg-positive exposure. HBIG and/or vaccination are reserved for non-responders, incompletely vaccinated, or those with unknown antibody status.

    Reference: CDC Updated PHS Guidelines for Management of Occupational Exposures to HBV, HCV, and HIV (2013); MMWR

  2. Question 2 · Hematology

    In differentiating acute monocytic leukemia from acute myeloblastic leukemia, a pair of esterase stains is often used. Which cytochemical pattern best supports a monocytic lineage?

    1. APositive specific (chloroacetate) esterase and negative nonspecific esterase
    2. BPositive nonspecific (alpha-naphthyl butyrate) esterase that is inhibited by sodium fluoride
    3. CPositive periodic acid-Schiff (PAS) in a coarse block pattern
    4. DPositive Prussian blue staining of the cytoplasm
    Show answer and explanation

    Correct answer: B. Positive nonspecific (alpha-naphthyl butyrate) esterase that is inhibited by sodium fluoride

    Monocytes and their precursors show strong nonspecific esterase activity (alpha-naphthyl butyrate or acetate) that is characteristically inhibited by sodium fluoride, distinguishing them from granulocytes. Specific chloroacetate esterase marks the granulocytic (myeloblastic) series instead. Coarse block PAS positivity suggests lymphoblasts, and Prussian blue detects iron (siderotic granules/ring sideroblasts), not monocytic differentiation.

    Reference: Rodak's Hematology: Clinical Principles and Applications, 6th ed. (Elsevier, 2020), cytochemistry chapter

  3. Question 3 · Immunohematology (Blood Group Serology)

    When grading tube agglutination, hemolysis in the presence of complement-binding antibodies should be interpreted as which of the following?

    1. AA positive reaction equivalent in significance to agglutination
    2. BA negative reaction because no clumps are seen
    3. CAn invalid result requiring repeat with fresh cells only
    4. DRouleaux formation
    Show answer and explanation

    Correct answer: A. A positive reaction equivalent in significance to agglutination

    Hemolysis produced by a complement-activating antibody (for example anti-A, anti-B, or some anti-Jka/Jkb) indicates an antigen-antibody reaction and is recorded as a positive result, often as strong as or stronger than visible agglutination. Interpreting it as negative would miss clinically significant antibodies. It is a genuine reaction, not an invalid one, and it is unrelated to rouleaux, which is a pseudoagglutination that disperses with saline replacement.

    Reference: AABB Technical Manual, 20th edition, 2020

  4. Question 4 · Urinalysis & Body Fluids

    A post-vasectomy patient submits a semen sample to confirm sterility. Which examination finding is required before the specimen can be reported as consistent with a successful vasectomy?

    1. AAbsence of spermatozoa confirmed on examination of a centrifuged specimen
    2. BPresence of fructose in the seminal plasma
    3. CNormal semen volume greater than 1.5 mL
    4. DPresence of at least 15 million sperm/mL
    Show answer and explanation

    Correct answer: A. Absence of spermatozoa confirmed on examination of a centrifuged specimen

    Post-vasectomy semen analysis aims to confirm azoospermia; because sperm may be sparse, the specimen (or its pellet after centrifugation) must be examined and reported as showing no spermatozoa. A sperm concentration of 15 million/mL is a fertility reference value, not a sterility criterion, and volume or fructose (which reflects seminal vesicle function) do not confirm vasectomy success.

    Reference: WHO Laboratory Manual for the Examination and Processing of Human Semen, 6th ed. (2021)

  5. Question 5 · Immunology & Serology

    A patient with suspected connective tissue disease has an ANA showing a homogeneous (diffuse) staining pattern by indirect immunofluorescence. This pattern is classically associated with antibodies against:

    1. ANucleolar RNA
    2. BCytoplasmic Jo-1 antigen
    3. CCentromere proteins
    4. DdsDNA and histones (deoxyribonucleoprotein)
    Show answer and explanation

    Correct answer: D. dsDNA and histones (deoxyribonucleoprotein)

    The homogeneous ANA pattern reflects antibodies to dsDNA and histones (nucleoprotein) and is seen in SLE and drug-induced lupus. A nucleolar pattern suggests scleroderma, a discrete speckled/centromere pattern suggests limited scleroderma (CREST), and anti-Jo-1 is a cytoplasmic antibody linked to polymyositis.

    Reference: Turgeon, Immunology & Serology in Laboratory Medicine, 7th ed., 2022

  6. Question 6 · Clinical Chemistry

    Therapeutic drug monitoring is most clinically valuable for drugs that have which characteristic?

    1. AA wide therapeutic index and predictable dose-response
    2. BA narrow therapeutic index where toxic and effective concentrations are close together
    3. CNo relationship between serum concentration and effect
    4. DRapid complete metabolism to inactive products within minutes
    Show answer and explanation

    Correct answer: B. A narrow therapeutic index where toxic and effective concentrations are close together

    TDM is most useful for drugs with a narrow therapeutic index (e.g., digoxin, phenytoin, aminoglycosides, lithium, theophylline), where the effective and toxic concentrations are close and small dosing changes can cause toxicity or treatment failure. Drugs with a wide margin or no concentration-effect relationship gain little from monitoring.

    Reference: Tietz Textbook of Clinical Chemistry and Molecular Diagnostics, 6th ed., 2018

  7. Question 7 · Microbiology

    As part of media quality control, a technologist inoculates a new lot of MacConkey agar with a stock strain to confirm the inhibition of Gram-positive growth. Which organism is the most appropriate QC strain for this specific purpose?

    1. AEscherichia coli ATCC 25922 (expected growth, pink)
    2. BEnterococcus faecalis ATCC 29212 (expected partial to no growth)
    3. CPseudomonas aeruginosa ATCC 27853 (expected colorless growth)
    4. DProteus mirabilis (expected swarming)
    Show answer and explanation

    Correct answer: B. Enterococcus faecalis ATCC 29212 (expected partial to no growth)

    To verify the selective (inhibitory) property of MacConkey agar, a Gram-positive control such as Enterococcus/Staphylococcus is used to confirm partial or complete inhibition. E. coli and P. aeruginosa are Gram-negative growth controls that confirm the medium supports growth and differentiates fermenters, not the inhibitory property. Proteus swarming is not the intended QC endpoint for selectivity.

    Reference: CLSI M22, Quality Control for Commercially Prepared Microbiological Culture Media (2018)

  8. Question 8 · Blood Banking & Transfusion Services

    A patient with recurrent severe allergic/anaphylactic reactions to plasma proteins and documented IgA deficiency requires red cells. Which product modification is most appropriate?

    1. AIrradiated red cells
    2. BWashed red cells
    3. CCMV-negative red cells
    4. DFrozen-thawed red cells only for storage
    Show answer and explanation

    Correct answer: B. Washed red cells

    Washed red cells have the residual plasma proteins (including IgA) removed, making them the product of choice for patients with severe allergic/anaphylactic reactions or IgA deficiency with anti-IgA. Irradiation prevents TA-GVHD, CMV-negative units reduce CMV risk, and freezing/deglycerolizing is primarily for rare-unit storage though it also washes plasma.

    Reference: AABB Technical Manual, 20th ed.; Circular of Information (2021)

  9. Question 9 · Coagulation & Hemostasis

    Platelet aggregation studies show an absent primary and secondary wave with ADP, collagen, and epinephrine, but a normal response to ristocetin. This pattern is most consistent with which disorder?

    1. ABernard-Soulier syndrome
    2. BGlanzmann thrombasthenia
    3. CVon Willebrand disease
    4. DStorage pool disease
    Show answer and explanation

    Correct answer: B. Glanzmann thrombasthenia

    Glanzmann thrombasthenia is a defect of platelet glycoprotein IIb/IIIa, which mediates fibrinogen-dependent aggregation; therefore aggregation to ADP, collagen, and epinephrine is absent while ristocetin agglutination (GPIb/vWF dependent) is preserved. Bernard-Soulier and vWD show the opposite pattern (absent ristocetin response), and storage pool disease typically shows a blunted second wave.

    Reference: Rodak's Hematology, 6th ed., 2020; platelet function testing guidelines

  10. Question 10 · General Laboratory, Quality Management & Safety

    A gray-top tube containing sodium fluoride and potassium oxalate is used primarily to preserve which analyte, and by what mechanism does the fluoride act?

    1. AGlucose; fluoride inhibits glycolytic enzymes such as enolase
    2. BCalcium; fluoride chelates calcium ions
    3. CPotassium; fluoride prevents cellular potassium leakage
    4. DLactate; fluoride activates lactate dehydrogenase
    Show answer and explanation

    Correct answer: A. Glucose; fluoride inhibits glycolytic enzymes such as enolase

    Sodium fluoride is an antiglycolytic agent that inhibits enolase in the glycolytic pathway, preserving glucose in the specimen; potassium oxalate acts as the anticoagulant by binding calcium. Fluoride does not chelate calcium (oxalate does that), does not prevent potassium leakage, and inhibits rather than activates glycolytic enzymes.

    Reference: Burtis & Bruns, Tietz Fundamentals of Clinical Chemistry and Molecular Diagnostics, 8th ed. (2019)

  11. Question 11 · Hematology

    Which feature most reliably favors a reactive/benign leukocytosis over an acute leukemia on a peripheral smear?

    1. AUniform population of cells with fine chromatin and prominent nucleoli
    2. BAuer rods within immature cells
    3. CPresence of a spectrum of maturing granulocytic forms without a blast excess
    4. DMarked thrombocytopenia with circulating blasts
    Show answer and explanation

    Correct answer: C. Presence of a spectrum of maturing granulocytic forms without a blast excess

    A reactive (leukemoid) response typically shows a complete spectrum of maturing granulocytes (myelocytes, metamyelocytes, bands, segmented) with few or no blasts and often toxic changes. A monomorphic immature population with open chromatin and nucleoli, Auer rods, or blasts with thrombocytopenia point instead to acute leukemia.

    Reference: Rodak's Hematology: Clinical Principles and Applications, 6th ed. (2020)

  12. Question 12 · Microbiology

    An enzyme-linked immunosorbent assay (ELISA) detecting IgM antibody to a virus is positive in a patient with an acute febrile illness. What does the presence of specific IgM most strongly indicate?

    1. ALong-standing immunity from remote past infection
    2. BRecent or acute/current infection
    3. CSuccessful vaccination years earlier
    4. DAbsence of any infection
    Show answer and explanation

    Correct answer: B. Recent or acute/current infection

    Virus-specific IgM antibodies appear early and are the first immunoglobulin produced in a primary immune response, so a positive IgM indicates recent or acute infection. IgG, not IgM, reflects past infection or vaccine-induced long-term immunity. A positive IgM does not indicate absence of infection. Detecting IgM is used to identify current/recent viral infection.

    Reference: Murray et al., Medical Microbiology, 9th ed. (Elsevier, 2021)

Medical Laboratory Technologist reference books and guidelines

Every question in this bank names the textbook or guideline its answer rests on. These are the sources our Medical Laboratory Technologist questions cite most often - the reading list to revise from alongside the bank.

Textbooks

10
  1. 1

    Rodak's Hematology: Clinical Principles and Applications

    6th edition2020
  2. 2

    Tietz Fundamentals of Clinical Chemistry and Molecular Diagnostics

    8th edition2019
  3. 3

    AABB Technical Manual

    20th edition
  4. 4

    Strasinger & Di Lorenzo, Urinalysis and Body Fluids

    7th edition2021
  5. 5

    Turgeon, Immunology & Serology in Laboratory Medicine

    7th edition2022
  6. 6

    WFH Guidelines for the Management of Hemophilia

    3rd edition2020
  7. 7

    ICSH Recommendations / Rodak's Hematology

    6th edition2020
  8. 8

    AABB Standards for Blood Banks and Transfusion Services

    33rd edition2022
  9. 9

    WHO Laboratory Manual for the Examination and Processing of Human Semen

    6th edition2021
  10. 10

    Tille, Bailey & Scott's Diagnostic Microbiology

    15th edition

Guidelines and standards

6
  1. 1

    NFPA 10 Standard for Portable Fire Extinguishers

    2022
  2. 2

    ISTH mixing study recommendations

    2020
  3. 3

    ASPEN Clinical Guidelines on trace elements

    2012
  4. 4

    SAMHSA Mandatory Guidelines for Federal Workplace Drug Testing Programs

    2017
  5. 5

    CDC Sexually Transmitted Infections Treatment Guidelines

    2021
  6. 6

    CDC Updated PHS Guidelines for Management of Occupational Exposures to HBV, HCV, and HIV

    2013

Where your regulator publishes a reading list, use the editions it names. Exam questions are not taken from any one book.

Last reviewed September 2026

About these questions: every question is original, researched by Neelim's exam research team, written to the published blueprint, with a rationale and a reference. No recalled or leaked exam content is used. How we write our questions.

Frequently asked questions

Are these real Medical Laboratory Technologist exam questions?
No. Every item is original, researched by Neelim's exam research team against the exam blueprint published by the health authorities. Real, recalled or leaked exam content breaches the testing bodies' rules and can lead to a permanent exam ban - we do not sell it, and neither should anyone else.
How many questions are in the Medical Laboratory Technologist bank?
Every bank starts at 3 full-length papers of roughly 150 questions each, the same length as the real computer-based exam, and you can add papers up to 6, including a bonus paper of our hardest questions. The papers do not overlap, so every question is new, and together they cover every sub-topic in the published blueprint.
What is the pass mark for the DHA Medical Laboratory Technologist exam?
50%. DHA publishes the pass score for each exam, and 50% is the figure for Medical Laboratory Technologist (LAB5631) in the DHA CBT Guideline, Sep 2026. The result is posted to your Sheryan account as Pass or Fail only - your score is not shared. Elsewhere in the GCC: DOH Pass / fail only, SCFHS 530 on a 200-800 scale, QCHP 50%, OMSB 55%, Kuwait MOH 60%.
How many questions are in the DHA Medical Laboratory Technologist exam, and how long is it?
150 multiple-choice questions in 3 hours, and the time includes registration and the introduction. It is a computer-based test delivered by Prometric at test centres in the UAE and abroad.
How much does the DHA Medical Laboratory Technologist exam cost?
USD 240 (about AED 880) per attempt, paid again for every re-sit. DHA also charges a flat AED 200 credentialing fee through Sheryan.
How many attempts do I get?
In the UAE, three in total across DHA, DOH, MOHAP and SHA, not three each, under clause 1.5.4 of the Unified PQR (April 2025). Clause 1.5.5 allows one further attempt with a different authority, except on the Consultant route. Elsewhere in the GCC: SCFHS up to 4 a year, QCHP 5 per scope, OMSB no set maximum, Kuwait MOH 3, 6 weeks apart.
Does this cover DHA, DOH, MOHAP, SCFHS and the other GCC regulators?
Yes, and it is not a generic set. Tell us which regulator you are sitting and we send the bank prepared for that authority's exam: its blueprint, its exam length and pass mark, and its local regulations. The core clinical knowledge is shared across the GCC; what changes by regulator is the test vendor (Prometric for DHA, SCFHS, QCHP, NHRA, Kuwait MOH; Pearson VUE for DOH, OMSB), the exam length, the pass mark, the local-regulation questions and, at some regulators such as DOH, an added oral or OSCE component. The table on this page shows each regulator's published format, pass mark and fee, and says where a figure is not published.
How do I receive it?
As PDF files. Card checkout is being set up, so for now you request it from this page and we send it to you directly, usually the same day.

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