QMS in Pharmaceutical industry l Quality Management system in Pharma Industry l Question & answers
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- Опубликовано: 30 сен 2024
- QMS in Pharmaceutical industry l Quality Management system in Pharmaceutical Industry l Question and answers
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Pick your favourite topic video from below playlist:
1. QMS - Quality Management System in Pharmaceutical industry : • QMS - Quality Manageme...
2. QA- Quality assurance in Pharmaceutical industry. : • QA- Quality assurance ...
3. QC - Quality Control in Pharmaceutical industry :
• QC - Quality Control i...
4. OSD - Tablet Manufacturing in Pharmaceutical industry :
• OSD - Tablet Manufactu...
5. Injectable processing - Injectable processing or Sterile dosage formulation : • Injectable processing ...
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Questions covered:
Q. What is a Quality Management System (QMS) ?
Q. What are the key elements of a QMS in the pharmaceutical sector ?
Q. How does a pharmaceutical QMS ensure compliance with regulatory requirements ?
Q. Explain the concept of risk management in QMS ?
Q. What role does validation play in pharmaceutical QMS ?
Q. How is change control implemented in a pharmaceutical QMS ?
Q. What is the purpose of a Master Validation Plan (MVP) in QMS ?
Q. Explain the significance of Good Documentation Practices (GDP) in QMS ?
Q : Which are the advance investigation tools commonly used in Pharmaceutical industry?
Q. Explain the purpose of a Quality Risk Management (QRM) process in a pharmaceutical QMS ?
Q. What is the difference between corrective action and preventive action in QMS ?
Q : What are the major four types of validation ?
Q. How does a pharmaceutical QMS address deviations from standard operating procedures (SOPs)?
Q. Explain the concept of Critical Quality Attributes (CQAs) in the context of pharmaceutical QMS?
Q. How does a pharmaceutical QMS handle the qualification of equipment and utilities?
Q. Explain the concept of CAPA effectiveness checks in QMS?
Q. What is the role of a Document Control System in a pharmaceutical QMS?
Q. How does a pharmaceutical QMS address complaints and recalls ?
Q. Explain the concept of Change Management in QMS.
Q. What is the role of a Quality Risk Management Plan in pharmaceutical QMS?
Q. How does a pharmaceutical QMS ensure data integrity in electronic systems?
Q. Explain the concept of Continuous Process Verification (CPV) in a pharmaceutical QMS.
Q. What is the purpose of a Stability Program in the QMS of a pharmaceutical company ?
Q. What is the role of Key Performance Indicators (KPIs) in monitoring the effectiveness of a pharmaceutical QMS ?
Q: What is the role of Standard Operating Procedures (SOPs) in pharmaceutical quality system ?
Q: What is the role of Training in maintaining quality system ?
Q. What does ALCOA plus stand for in data integrity?
Q. What is Deviation?
Q : Which are the simple investigation tools commonly used in Pharmaceutical industry?
Q. How do you classify deviations?
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Keywords to find this video:
pharmaceutical industry,change control in pharmaceutical industry,data integrity in pharmaceutical industry,process validation in pharmaceutical industry,validation in pharmaceutical industry,quality control in the pharmaceutical industry,quality assurance in pharmaceutical industry,quality assurance jobs in pharmaceutical industry,quality assurance interview questions and answers,gmp in pharmaceutical industry,quality management system
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Jessika Forges
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Very informative. Thank you!
Thanks🙏
@@PharmGrow what is SME tell me
@@chintu4972 Subject matter expert ( Person having detail knowledge about that specific topic)
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good job
Thanks
Thank you so much
You're most welcome