Good Manufacturing practices (GMP) in Pharmaceutical industry l 15 important Question and answers

Good Manufacturing practices (GMP) in Pharmaceutical industry l 15 basic and important Interview Question
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Questions covered:
Q. : What are Good Manufacturing Practices (GMP) in the pharmaceutical industry?
Q. : Why are Good Manufacturing Practices important for ensuring product quality and safety?
Q. : What are the key components of GMP guidelines?
Q. : How do GMP regulations impact the manufacturing processes in the pharmaceutical industry?
Q. : What are some common challenges in maintaining compliance with GMP requirements?
Q. : How do you ensure cleanliness and hygiene in a pharmaceutical manufacturing facility?
Q. : What is the role of documentation in GMP compliance?
Q. : Can you provide an example of a situation where adherence to GMP helped prevent a manufacturing issue or ensure product quality?
Q. : How do you handle equipment qualification and validation in GMP?
Q. : What measures do you take to ensure proper storage and handling of raw materials and finished products in accordance with GMP?
Q. : How do you address deviations or non-conformances in the manufacturing process while maintaining GMP compliance?
Q. : What are the requirements for personnel training and qualifications in GMP?
Q. : How do you ensure traceability and accountability in the manufacturing process according to GMP?
Q. : What are the steps involved in conducting a thorough GMP audit or self-inspection?
Q. : Can you discuss the role of quality control and quality assurance in GMP compliance?

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