Calibration in Pharmaceutical industry l 21 basic and important Interview Question and answers

Calibration in Pharmaceutical industry l 21 basic and important Interview Question and answers
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Questions covered:
Q. : What is calibration, and why is it essential in the pharmaceutical industry?
Q. How often should equipment be calibrated or what should be the calibration frequency in the pharmaceutical industry?
Q. What are the main parameters that require calibration in the pharmaceutical industry?
Q. What is the basic difference between calibration and validation?
Q. How do you handle out-of-calibration situations for critical equipment ?
Q. What are calibration standards, and why are they important?
Q. Whether calibration of instrument can be outsourced i.e. can be done external agency, and what are the considerations?
Q. How does calibration support data integrity in pharmaceutical processes?
Q. How do you ensure environmental factors don't affect calibration results?
Q. What is traceability, and why it is crucial or important in calibration?
Q. How do you document the calibration process, and why is documentation important?
Q. What are common challenges faced during the calibration process in the pharmaceutical industry?
Q. How you prioritize instruments for calibration in a large pharmaceutical facility?
Q. How can calibration support compliance with Good Manufacturing Practices (GMP)?
Q. Explain the difference between in-house and off-site calibration services?
Q. How do you ensure that calibration equipment itself remains accurate and reliable?
Q. What is the process for handling calibration-related deviations?
Q. What is relationship between calibration and process validation?
Q. How to deal with instruments that consistently fail in calibration?
Q. How does calibration contribute to product quality and patient safety?
Q. What role does risk assessment play in determining calibration frequencies?

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