Quality Assurance in Pharmaceutical industry l 30 Interview Question and answers
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1. QMS - Quality Management System in Pharmaceutical industry :    • QMS - Quality Management System in Ph...  
2. QA- Quality assurance in Pharmaceutical industry. :    • QA- Quality assurance in Pharmaceutic...  
3. QC - Quality Control in Pharmaceutical industry :    • QC - Quality Control in Pharmaceutica...  
4. OSD - Tablet Manufacturing in Pharmaceutical industry :    • OSD - Tablet Manufacturing in Pharmac...  
5. Injectable processing - Injectable processing or Sterile dosage formulation :    • Injectable processing - Injectable pr...  

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Questions covered:
Q: What is the primary objective of quality assurance in the pharmaceutical industry?
Q: Which international organization provides guidelines for Good Manufacturing Practice (GMP) in the pharmaceutical industry?
Q: What is the role of process capability analysis in pharmaceutical manufacturing?
Q: How does the pharmaceutical industry manage the qualification and validation of cleaning processes?
Q: What are the guidelines for conducting qualification of analytical instruments used in quality control?
Q: How is risk-based validation applied in the pharmaceutical industry?
Q: What is the role of validation master plans (VMPs) in pharmaceutical manufacturing?
Q: How is the qualification of utilities and facilities managed in the pharmaceutical industry?
Q: What are the guidelines for environmental monitoring in pharmaceutical manufacturing areas?
Q: How does the pharmaceutical industry handle the storage and handling of reference standards?
Q: What is the purpose of conducting process performance qualification (PPQ) in pharmaceutical manufacturing?
Q: How are critical quality attributes (CQAs) determined for pharmaceutical products?
Q: What is the process for handling product Quality Risk Management (QRM) during pharmaceutical development?
Q: How does the pharmaceutical industry manage the qualification of contract manufacturers and third-party suppliers?
Q. What are the requirements for conducting process validation of analytical methods in pharmaceutical quality control?
Q: How are manufacturing deviations and investigations documented and managed?
Q: What is the role of quality risk management in selecting appropriate starting materials for drug manufacturing?
Q: What are the guidelines for conducting risk-based environmental monitoring in pharmaceutical manufacturing areas?
Q: How does the pharmaceutical industry manage the qualification of critical suppliers?
Q. What are the key considerations for developing a Quality Culture in the pharmaceutical industry?

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