IPQA Interview Question Quiz 2 Posted on August 7, 2023August 7, 2023 By Shiv Kumar 33 Created on August 07, 2023 By Shiv Kumar IPQA Interview Question Quiz 2 In Process Quality Assurance, IPQA is very important in any manufacturing of pharmaceutical Industries, primary role is to ensure that the manufacturing process adheres to cGMP guidelines and follows the approved standard operating procedures. also, review batch records and documentation to ensure accuracy and completeness. The Main Objective of IPQA is to maintain product quality and ensure that all finished products meet the required specifications 1 / 10 Question 1: What type of documentation does an IPQA officer review to ensure accuracy and completeness of BMR? Batch records and IPQA reports. Production Planing Good receipt Note None 2 / 10 Question 2: What does an IPQA officer do when a manufacturing process is out of control? Take immediate action to bring the process back under control and within predefined specifications. Take immediate action to bring inform security Immediate inform to engineering None 3 / 10 Question 3: How does an IPQA officer stay updated on the latest industry regulations and guidelines? Attending industry seminars, workshops, and subscribing to regulatory agencies' newsletters. Reading the current regulatory Guidelines updates Attending GMPs Training All of the above 4 / 10 Question 4: What is the purpose of conducting risk assessments in IPQA activities? To identify and prioritize potential risks to product quality. To make simplify production planning For better Inventory Control None 5 / 10 Question 5: What is the primary goal of IPQA activities during the manufacturing process? Ensuring product quality and compliance with regulations. Production Planning and Target Completion Transport Validation None 6 / 10 Question 6: What are the consequences of non-compliance with cGMP guidelines during manufacturing? Potential product recalls, regulatory actions, and impact on patient safety. Production Planning and Target Achievement Finished Product Dispatch to Market None 7 / 10 Question 7: What is the purpose of conducting routine inspections on the manufacturing floor? To verify that each step of the manufacturing process is executed correctly. To identify the Gaps between the actual vs written approved Procedures. To compliance with specification and written approved Procedures. All of the above 8 / 10 Question 8: How does an QA officer handle deviations and non-conformances in the manufacturing process? Investigate the root cause, initiate a deviation report, and implement corrective and preventive actions. Review, evaluation and login analyze the risk and evaluate impact of deviation in consultation with HOD of responsible department All of the above 9 / 10 Question 9 : What are In process checks? Checks carried out during an activity to monitor To ensure that the product conforms to its specification Both of the above Production Target Completion 10 / 10 Question 10 : Which class of Area is Required for Tablets and Capsule Manufacturing? Class D Class B Class A Class C Your score isThe average score is 81% LinkedIn Facebook VKontakte 0% Restart quiz Uncategorized