Clinical Biochemistry Prometric exam questions with answers
15 original practice questions written to the Clinical Biochemistry exam blueprint, each with the answer and why the other options are wrong. Below them: the Clinical Biochemistry 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
- 12
- Questions in the free mock
Quick answer
The Clinical Biochemistry exam is 150 MCQs in 3 hours at DHA (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 12-question timed mock.
The Clinical Biochemistry exam in every GCC country
DHA publish an exact Clinical Biochemistry exam; the others apply one format to every title. Figures come from each regulator's own exam pages - anything not published says so.
| Regulator | Exam | Format | Pass mark | Fee per attempt | Practise |
|---|---|---|---|---|---|
| DHA Dubai | Clinical Biochemistry Technologist (BIC5661) | 150 MCQs in 3 hours | 50% | USD 240 (about AED 880) | DHA questions → |
| DOH Abu Dhabi, Al Ain and Al Dhafra | DOH licensing exam Regulator-wide format | Written + oral/OSCE | Pass / fail only | Not published | DOH questions → |
| MOHAP Northern Emirates - Ajman, Umm Al Quwain, Ras Al Khaimah and Fujairah | MOHAP licensing exam Regulator-wide format | Computer-based | Not published | Not published | MOHAP questions → |
| SHA Emirate of Sharjah | SHA licensing exam Regulator-wide format | Set at assessment | Not published | Not published | SHA questions → |
| SCFHS Kingdom of Saudi Arabia | SCFHS licensing exam Regulator-wide format | 200 MCQs, 240 min | 500-560 of 800 | Not published | SCFHS questions → |
| QCHP State of Qatar | QCHP licensing exam Regulator-wide format | 150 MCQs, 3 hrs | 50-65% | Not published | QCHP questions → |
| NHRA Kingdom of Bahrain | NHRA licensing exam Regulator-wide format | Prometric CBT | Not published | Not published | NHRA questions → |
| OMSB Sultanate of Oman | OMSB licensing exam Regulator-wide format | Computer-based OC exam | Not published | Not published | OMSB questions → |
| Kuwait MOH State of Kuwait | Kuwait MOH licensing exam Regulator-wide format | 150 MCQs, 170 min | 60-70% | Not published | Kuwait MOH questions → |
exact exam published for Clinical Biochemistry
Pass marks, attempts and fees change - confirm yours on the regulator's exam page before you book.
15 Clinical Biochemistry 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.
- Question 1Analytical techniques and instrumentationmedium
A patient with severe hypertriglyceridaemia has sodium 124 mmol/L on the main analyser, which uses indirect ion-selective electrodes. A blood gas analyser gives 139 mmol/L. What explains the difference?
- ADirect ISEs are affected by haemolysis
- BSodium is lost from the sample by evaporation
- CThe blood gas analyser uses flame photometry
- DIndirect ISE dilution error from increased lipid volume
Show answer and explanation
Answer: D. Indirect ISE dilution error from increased lipid volume
Indirect ISEs dilute the sample and assume normal plasma water content; excess lipid or protein reduces water fraction and causes pseudohyponatraemia. Direct ISEs measure activity in plasma water and are unaffected.
- Question 2Carbohydrate, lipid and cardiac biochemistryhard
A patient has a high-sensitivity troponin above the 99th percentile on two samples with no change between them. There are no symptoms or ECG changes of ischaemia. How should this be classified?
- AChronic myocardial injury
- BAcute myocardial infarction
- CAcute non-ischaemic injury
- DNormal troponin result
Show answer and explanation
Answer: A. Chronic myocardial injury
Myocardial injury is troponin above the 99th percentile upper reference limit; it is acute if there is a rise or fall and chronic if stable. Myocardial infarction requires acute injury plus clinical evidence of ischaemia.
- Question 3Carbohydrate, lipid and cardiac biochemistrymedium
A fasting lipid profile shows total cholesterol 6.0, HDL 1.2 and triglyceride 2.2 mmol/L. What is the calculated LDL cholesterol?
- A2.6 mmol/L
- B4.8 mmol/L
- C3.8 mmol/L
- D3.0 mmol/L
Show answer and explanation
Answer: C. 3.8 mmol/L
Friedewald in mmol/L: LDL = TC - HDL - TG/2.2 = 6.0 - 1.2 - 1.0 = 3.8 mmol/L. The formula is invalid when triglycerides exceed about 4.5 mmol/L.
- Question 4Endocrinologymedium
In an overnight 1 mg dexamethasone suppression test for Cushing syndrome, which morning cortisol result indicates failure of suppression?
- ABelow 50 nmol/L
- BBelow 20 nmol/L
- CAbove 50 nmol/L
- DExactly 100 nmol/L only
Show answer and explanation
Answer: C. Above 50 nmol/L
A 09:00 cortisol above 50 nmol/L (1.8 microgram/dL) after 1 mg dexamethasone at midnight indicates failure to suppress and needs further testing. Oral oestrogens and enzyme-inducing drugs can cause false positives.
- Question 5Quality control and method evaluationeasy
A single internal quality control result falls 3.4 SD above the mean. What should happen under Westgard rules?
- AReject the run as a 1-3s violation
- BAccept the run as a warning only
- CAccept if the next control is in range
- DAverage with the previous control
Show answer and explanation
Answer: A. Reject the run as a 1-3s violation
A single control exceeding the mean by more than 3 SD violates the 1-3s rejection rule, usually indicating random error, and patient results should not be released until the problem is fixed. The 1-2s rule is the warning rule.
- Question 6Liver, gastrointestinal and pancreatic functionmedium
A healthy 22-year-old has mild jaundice during a fasting period. Bilirubin is 45 micromol/L, mostly unconjugated, with normal liver enzymes and no haemolysis. What is the most likely diagnosis?
- ADubin-Johnson syndrome
- BPrimary biliary cholangitis
- CCrigler-Najjar type 1
- DGilbert syndrome
Show answer and explanation
Answer: D. Gilbert syndrome
Gilbert syndrome causes mild unconjugated hyperbilirubinaemia that rises with fasting or illness, with normal enzymes and no haemolysis. Dubin-Johnson causes conjugated hyperbilirubinaemia, and Crigler-Najjar type 1 presents with severe neonatal jaundice.
- Question 7Quality control and method evaluationhard
A laboratory is establishing a new reference interval by the non-parametric method. What is the recommended minimum number of healthy reference individuals?
- A20 individuals
- B120 individuals
- C40 individuals
- D60 individuals
Show answer and explanation
Answer: B. 120 individuals
CLSI recommends at least 120 reference individuals per partition to estimate the 2.5th and 97.5th percentiles non-parametrically. Twenty samples are used for verifying, not establishing, a transferred interval.
- Question 8Renal function, electrolytes and acid-baseeasy
A patient has sodium 140, chloride 100 and bicarbonate 24 mmol/L. What is the anion gap?
- A40 mmol/L
- B64 mmol/L
- C8 mmol/L
- D16 mmol/L
Show answer and explanation
Answer: D. 16 mmol/L
Anion gap = Na - (Cl + HCO3) = 140 - 124 = 16 mmol/L. Adding potassium changes the result, so laboratories should state which formula they use.
Halfway - how are you scoring?
Test yourself under real exam conditions
The free 12-question mock is timed and scored against the pass mark, domain by domain, so you see exactly where you are losing marks. The full Clinical Biochemistry bank has 3 full-length papers (about 450 questions) for AED 249, one-time.
- Question 9Pre-analytical factors, laboratory safety and ethicsmedium
A potassium of 6.9 mmol/L is found on a ward sample with no haemolysis. What is the correct action?
- ARelease it electronically and wait for the ward to see it
- BHold the result until the next day's batch
- CRepeat the test three times before reporting
- DPhone the result to a responsible clinician and document it
Show answer and explanation
Answer: D. Phone the result to a responsible clinician and document it
Critical results must be communicated promptly to a responsible clinician by phone, with read-back confirmation and documentation of who received it and when. Electronic release alone may not be seen in time.
- Question 10Proteins, therapeutic drug monitoring and toxicologymedium
Serum protein electrophoresis shows a discrete band in the gamma region. What is the next laboratory step?
- AImmunofixation to type the paraprotein
- BRepeat electrophoresis in 6 months only
- CMeasure C-reactive protein
- DMeasure serum albumin
Show answer and explanation
Answer: A. Immunofixation to type the paraprotein
A discrete band suggests a monoclonal paraprotein, which is characterised by immunofixation and quantified, often with serum free light chains. Monitoring without typing misses the diagnosis.
- Question 11Quality control and method evaluationmedium
In one run, the level 1 control is 2.2 SD above its mean and the level 2 control is 2.1 SD below its mean. Which rule is violated and what does it indicate?
- A2-2s, indicating systematic error
- B4-1s, indicating systematic error
- CR-4s, indicating random error
- D10x, indicating a trend
Show answer and explanation
Answer: C. R-4s, indicating random error
A range of more than 4 SD between two controls in the same run violates R-4s and suggests random error, such as pipetting problems or bubbles. The 2-2s rule needs both controls on the same side.
- Question 12Renal function, electrolytes and acid-basemedium
A sample shows potassium 9.2 mmol/L, calcium 0.6 mmol/L and very low alkaline phosphatase in a well patient with a normal ECG. What is the most likely cause?
- ATrue hyperkalaemia from renal failure
- BDelayed separation at low temperature
- CContamination with K2EDTA
- DHypoparathyroidism with tetany
Show answer and explanation
Answer: C. Contamination with K2EDTA
Potassium EDTA contamination raises potassium and chelates calcium, magnesium and the zinc needed for ALP activity, producing this pattern. The sample should be rejected and recollected in the correct order of draw.
- Question 13Renal function, electrolytes and acid-basemedium
A bodybuilder with very high muscle mass has a creatinine-based eGFR of 55 mL/min/1.73 m2 but no other evidence of kidney disease. Which test helps confirm true kidney function?
- ARepeat creatinine after a meat meal
- BCystatin C-based eGFR
- CUrine sodium concentration
- DSerum urea alone
Show answer and explanation
Answer: B. Cystatin C-based eGFR
Creatinine depends on muscle mass and diet, so it can underestimate GFR in muscular people; cystatin C is less affected and is recommended for confirmation. A recent meat meal raises creatinine further.
- Question 14Renal function, electrolytes and acid-basemedium
A euvolaemic patient has serum sodium 125 mmol/L and serum osmolality 260 mOsm/kg, with normal thyroid and adrenal function. Which urine findings support SIADH?
- AUrine osmolality below 100 and urine sodium below 20
- BUrine osmolality above 100 and urine sodium above 30
- CUrine osmolality below 50 with high urine volume
- DUrine sodium below 10 with high specific gravity
Show answer and explanation
Answer: B. Urine osmolality above 100 and urine sodium above 30
SIADH shows inappropriately concentrated urine (osmolality above 100 mOsm/kg) and urine sodium above 30 mmol/L in a euvolaemic patient with hypotonic hyponatraemia. Very dilute urine suggests excess water intake.
- Question 15Renal function, electrolytes and acid-basemedium
An arterial gas shows pH 7.50, PaCO2 6.5 kPa and bicarbonate 36 mmol/L. What is the primary disorder?
- ARespiratory alkalosis with renal compensation
- BMetabolic alkalosis with respiratory compensation
- CRespiratory acidosis with renal compensation
- DMixed metabolic and respiratory acidosis
Show answer and explanation
Answer: B. Metabolic alkalosis with respiratory compensation
Alkalaemia with raised bicarbonate indicates metabolic alkalosis, and the raised PaCO2 reflects compensatory hypoventilation. Respiratory alkalosis would show a low PaCO2.
What the Clinical Biochemistry exam covers
The blueprint groups questions into these domains. Weight your revision the same way - the heavier domains carry more of your score.
Analytical techniques and instrumentation
~14%Spectrophotometry and the Beer-Lambert law · Ion-selective electrodes · Immunoassay design
Quality control and method evaluation
~14%Internal quality control · Random versus systematic error · Precision, coefficient of variation and bias
Renal function, electrolytes and acid-base
~14%Creatinine, eGFR and cystatin C · Anion gap and osmolal gap · Hyponatraemia investigation
Liver, gastrointestinal and pancreatic function
~10%Patterns of liver function tests · Bilirubin metabolism and Gilbert syndrome · Alkaline phosphatase origin
Carbohydrate, lipid and cardiac biochemistry
~12%Diagnosis of diabetes · Glucose sample handling and glycolysis · HbA1c interferences
Endocrinology
~14%Thyroid function test patterns · Adrenal testing · Primary aldosteronism
Proteins, therapeutic drug monitoring and toxicology
~12%Serum protein electrophoresis, immunofixation and free light chains · Therapeutic drug monitoring · Paracetamol and salicylate measurement
Pre-analytical factors, laboratory safety and ethics
~10%Order of draw and tube additives · Haemolysis, lipaemia and icterus interference · Sample rejection and labelling standards
How to answer these questions
Questions test applied practice: what you would do with this patient, this result or this image - not textbook definitions.
Safety items (radiation, infection control, patient identification, equipment checks) are high-yield and quick to revise.
Under time pressure, flag and move on: every question carries the same mark.
Aim to score comfortably above your regulator's pass mark - 10 to 15 points of margin - on timed, full-length practice before you book.
Clinical Biochemistry exam questions: FAQs
How many questions are in the Clinical Biochemistry Prometric exam?
What is the pass mark for the Clinical Biochemistry exam?
Are these real exam questions?
Is the Clinical Biochemistry exam the same in every GCC country?
How should I use these questions?
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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