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ASQ CPGP Exam Syllabus Topics:

SectionWeightObjectives
Materials Systems13%-17%- Material controls
  • 1. Inventory control
  • 2. Supplier qualification
  • 3. Incoming material inspection
  • 4. Storage and distribution
Packaging and Labeling Systems5%-9%- Packaging controls
  • 1. Label issuance and reconciliation
  • 2. Tamper evidence
  • 3. Packaging inspections
Facilities and Equipment Systems18%-22%- Equipment
  • 1. Qualification and validation
  • 2. Calibration and maintenance
  • 3. Equipment cleaning
- Facilities
  • 1. Cleaning and sanitation
  • 2. Facility design and maintenance
  • 3. Utilities and environmental controls
Quality Management Systems22%-26%- Quality systems
  • 1. Quality culture
  • 2. Training systems
  • 3. GMP regulations and guidance
  • 4. Documentation systems
Production Systems23%-27%- Manufacturing operations
  • 1. Contamination control
  • 2. Packaging and labeling
  • 3. Batch processing
  • 4. Process validation
Laboratory Systems10%-14%- Laboratory operations
  • 1. Analytical testing
  • 2. Stability programs
  • 3. Data integrity
  • 4. Microbiology controls

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ASQ Certified Pharmaceutical GMP Professional Sample Questions (Q173-Q178):

NEW QUESTION # 173
In business continuity planning, the supply chain impact analysis aims to:
Response:

Answer: B


NEW QUESTION # 174
Which ISO standard is commonly referenced in the context of pharmaceutical quality management?
Response:

Answer: A


NEW QUESTION # 175
During scale-up, __________ principles guide the increase in production volume while maintaining product quality.
Response:

Answer: D


NEW QUESTION # 176
What action is crucial when receiving materials from unapproved suppliers?
Response:

Answer: B


NEW QUESTION # 177
Preventive maintenance of laboratory instruments is critical for:
Response:

Answer: C


NEW QUESTION # 178
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