Good warehousing practices and materials management MCQs With Answer provide B.Pharm students with essential knowledge on pharmaceutical storage, inventory control, and supply chain quality. This concise guide covers key concepts such as Good Warehousing Practices (GWP), GMP overlap, storage conditions, cold chain management, FIFO/FEFO, documentation, traceability, validation, pest control, and safety. Emphasis is on maintaining product integrity, regulatory compliance, and efficient materials handling to support quality assurance and patient safety. Practical topics include temperature mapping, quarantine procedures, batch segregation, labels, and computerized inventory systems. These MCQs reinforce learning and prepare students for real-world pharmacy operations. Now let’s test your knowledge with 30 MCQs on this topic.
Q1. Which principle ensures that the oldest stock is used before newer stock to minimize expiry losses?
- First Expiry First Out (FEFO)
- Last In First Out (LIFO)
- Random Access
- First In First Out (FIFO)
Correct Answer: First In First Out (FIFO)
Q2. What is the primary objective of Good Warehousing Practices (GWP) in pharmaceuticals?
- Maximize warehouse profits
- Ensure product safety, quality and traceability
- Reduce staff headcount
- Speed up manufacturing processes
Correct Answer: Ensure product safety, quality and traceability
Q3. Which of the following is a critical environmental parameter for temperature-sensitive drug storage?
- Lux level
- Relative humidity
- Magnetic field strength
- Sound level
Correct Answer: Relative humidity
Q4. What does FEFO stand for and when is it preferred over FIFO?
- First Expiry First Out; preferred for expiry-dated materials
- Fastest Entry Fast Out; preferred for bulk goods
- First Entry First Out; preferred for sterile items
- Final Expiry Final Out; preferred for long-term stock
Correct Answer: First Expiry First Out; preferred for expiry-dated materials
Q5. Which document specifies storage conditions, handling precautions, and shelf life for a pharmaceutical batch?
- Batch Manufacturing Record (BMR)
- Master Formula Card
- Certificate of Analysis (CoA)
- Material Safety Data Sheet (MSDS)
Correct Answer: Certificate of Analysis (CoA)
Q6. What is the purpose of quarantine area in a pharmaceutical warehouse?
- Store fast-moving products
- Temporary storage for incoming batches pending release
- Holding returned empty packaging
- Mixing different lots for uniformity
Correct Answer: Temporary storage for incoming batches pending release
Q7. Which practice improves traceability of materials in the warehouse?
- Manual tally sheets only
- Use of barcodes or RFID linked to batch records
- Storing everything on open pallets without labels
- Rotation of staff weekly
Correct Answer: Use of barcodes or RFID linked to batch records
Q8. In temperature mapping of a cold room, what is the main goal?
- Determine staff movement patterns
- Identify temperature distribution and hotspots/cold spots
- Measure electrical consumption of compressors
- Test alarm volume
Correct Answer: Identify temperature distribution and hotspots/cold spots
Q9. Which inventory control method uses safety stock and reorder point calculations?
- Kanban only
- Periodic review without calculations
- Continuous inventory control
- Just-in-case with no monitoring
Correct Answer: Continuous inventory control
Q10. What is a critical record to maintain for rejected or returned pharmaceutical batches?
- Stock transfer note
- Rejected material record with quarantine and disposition details
- Production schedule
- Payroll register
Correct Answer: Rejected material record with quarantine and disposition details
Q11. Which of these is a key element of materials handling safety in warehouses?
- Untrained use of forklifts to save time
- Regular equipment maintenance and staff training
- Stacking heavy loads on top levels without support
- Ignoring load capacity signs
Correct Answer: Regular equipment maintenance and staff training
Q12. What is the role of temperature and humidity monitoring systems in pharmaceutical storage?
- They provide cosmetic information only
- They ensure environmental conditions remain within validated limits and trigger alarms
- They replace the need for validation
- They are used only during inspections
Correct Answer: They ensure environmental conditions remain within validated limits and trigger alarms
Q13. Which regulatory concept overlaps with Good Warehousing Practices in pharmaceuticals?
- Good Manufacturing Practice (GMP)
- Good Agricultural Practice (GAP)
- Good Laboratory Practice (GLP)
- Good Clinical Practice (GCP)
Correct Answer: Good Manufacturing Practice (GMP)
Q14. What is the recommended action when a temperature excursion is detected for stored products?
- Ignore if short duration
- Investigate, record, assess impact on product quality, and take corrective action
- Immediately dispose of all stock without assessment
- Reset the alarm and continue normal operations
Correct Answer: Investigate, record, assess impact on product quality, and take corrective action
Q15. Which practice reduces the risk of cross-contamination in a pharmaceutical warehouse?
- Mixed storage of incompatible materials on the same shelf
- Segregated storage areas and dedicated equipment for incompatible substances
- Open bins for all materials
- Using the same cleaning cloths across areas
Correct Answer: Segregated storage areas and dedicated equipment for incompatible substances
Q16. What is the function of warehouse layout design in materials management?
- Maximize travel time for workers
- Optimize flow, minimize handling, and improve safety and traceability
- Increase storage of expired products
- Create confusing paths to secure stock
Correct Answer: Optimize flow, minimize handling, and improve safety and traceability
Q17. Which documentation supports the chain of custody for a pharmaceutical batch from receipt to dispatch?
- Only verbal confirmation
- Material receipt, inventory records, movement logs and dispatch documents
- Supplier marketing brochure
- Employee timesheets
Correct Answer: Material receipt, inventory records, movement logs and dispatch documents
Q18. For cold chain logistics, which element is essential to maintain product quality during transport?
- Insulated packaging and temperature-controlled vehicles with monitoring
- Standard cardboard boxes without insulation
- Storing products in sun-exposed vehicles
- Transport without documentation
Correct Answer: Insulated packaging and temperature-controlled vehicles with monitoring
Q19. Which KPI is commonly used to measure warehouse inventory accuracy?
- Order picking speed only
- Inventory accuracy percentage (system vs physical count)
- Number of forklifts
- Employee break times
Correct Answer: Inventory accuracy percentage (system vs physical count)
Q20. What is the importance of stability study data in determining warehouse storage conditions?
- It provides marketing claims
- It defines validated storage temperatures, humidity, and shelf life for products
- It is unrelated to storage
- It only applies to clinical trials
Correct Answer: It defines validated storage temperatures, humidity, and shelf life for products
Q21. Which of the following is a key step in receiving raw materials to ensure compliance?
- Immediate mixing without checks
- Verification against purchase order, visual inspection and sampling for testing
- Storing randomly in main warehouse
- Ignoring supplier documentation
Correct Answer: Verification against purchase order, visual inspection and sampling for testing
Q22. Which practice is essential to prevent pest infestation in pharmaceutical warehouses?
- Food allowed in storage aisles
- Regular pest control program and good housekeeping
- Leaving doors open at night
- Storing products directly on the floor
Correct Answer: Regular pest control program and good housekeeping
Q23. What is the role of validation in warehouse equipment like cold rooms and monitoring systems?
- Validation is optional for critical equipment
- To demonstrate equipment performs as intended and maintains required conditions
- Only for auditing aesthetics
- Replace routine maintenance
Correct Answer: To demonstrate equipment performs as intended and maintains required conditions
Q24. Which inventory method helps reduce holding costs by ordering only what is needed?
- Just-in-Time (JIT)
- Permanent overstocking
- Yearly bulk purchasing without review
- Random ordering
Correct Answer: Just-in-Time (JIT)
Q25. In materials management, what does batch segregation prevent?
- Efficient picking
- Mix-up of different lots and cross-contamination
- Faster shipping
- Accurate accounting only
Correct Answer: Mix-up of different lots and cross-contamination
Q26. Which action should be taken if a received material lacks a certificate of analysis?
- Accept and use immediately
- Place material in quarantine and request CoA from supplier before release
- Sell the material to another party
- Ignore documentation requirements
Correct Answer: Place material in quarantine and request CoA from supplier before release
Q27. Which technology enhances accuracy and speed of picking and reduces human errors?
- Paper-based picking lists only
- Voice picking, barcode scanning or RFID systems
- Random manual selection
- Handwritten labels without verification
Correct Answer: Voice picking, barcode scanning or RFID systems
Q28. What is a critical consideration when storing hazardous pharmaceutical materials?
- Store them in general finished-goods area
- Use dedicated, labeled, ventilated storage with safety data sheets accessible
- Combine with edible products storage
- Ignore PPE requirements for handlers
Correct Answer: Use dedicated, labeled, ventilated storage with safety data sheets accessible
Q29. Which practice supports regulatory inspections and product recalls?
- Poor documentation and missing batch records
- Robust record-keeping, traceability and batch segregation
- Discarding old records regularly
- Mixing records among employees
Correct Answer: Robust record-keeping, traceability and batch segregation
Q30. What is the best approach for disposal of expired or rejected pharmaceutical materials?
- Dispose without documentation
- Follow documented destruction procedures with witness, record and environmental compliance
- Dump into general waste bins
- Return to active inventory after dilution
Correct Answer: Follow documented destruction procedures with witness, record and environmental compliance

I am a Registered Pharmacist under the Pharmacy Act, 1948, and the founder of PharmacyFreak.com. I hold a Bachelor of Pharmacy degree from Rungta College of Pharmaceutical Science and Research. With a strong academic foundation and practical knowledge, I am committed to providing accurate, easy-to-understand content to support pharmacy students and professionals. My aim is to make complex pharmaceutical concepts accessible and useful for real-world application.
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