Aarti Drugs R&D Officer Interview Questions and Answers

How to sell medicine and conversation with Doctor.

Q1. Company role and responsibility
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Q1. Public presentation
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Good GDP,USP,FDA,CGMP.

Q1. Explain line clearence procedure
Ans. 
Line clearance procedure is a process followed in pharmaceutical manufacturing to ensure that equipment and areas are free from any previous product or contamination before starting a new production.
• Line clearance procedure is performed to prevent cross-contamination and ensure product quality.

• It involves a series of checks and documentation to verify that the equipment, area, and materials are ready for use.

• Line clear...read more
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Q2. What is difference between ANF and Nutch filter?
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ANF and Nutch filter are both used in the field of information retrieval, but they have different purposes and functionalities.
• ANF (Approximate Nearest Neighbor Filtering) is a technique used to efficiently filter out irrelevant data points in a dataset based on their proximity to a query point.

• Nutch filter, on the other hand, is a component of the Apache Nutch web crawler framework that is used to filter and prioritiz...read more
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Q3. Types of line clearence?
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There are three types of line clearance: equipment line clearance, product line clearance, and area line clearance.
• Equipment line clearance involves ensuring that all equipment used in a production line is properly cleaned and free from any previous product or material.

• Product line clearance involves verifying that the previous product has been completely removed from the production line before starting a new product.

• A...read more
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Q4. Explain difficulties during line clearence
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Difficulties during line clearance include time constraints, equipment availability, and potential contamination risks.
• Time constraints can make it challenging to thoroughly clean and inspect the production line before starting a new batch.

• Limited availability of cleaning equipment or resources can hinder the efficiency of line clearance.

• There is a risk of cross-contamination if residues or contaminants from the previo...read more
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Q5. What are types of observations and how they are classified?
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Observations can be classified as critical, major, or minor based on their impact on quality and compliance.
• Critical observations have a significant impact on product quality and regulatory compliance.

• Major observations have a moderate impact on product quality and regulatory compliance.

• Minor observations have a minimal impact on product quality and regulatory compliance.

• Observations can be related to equipment, proces...read more
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Q6. SAP related batch release, usage decision,batch no allotting,QA issuance?
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Q1. Tell me about yourself?
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Q2. Salery discussion?
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Q1. Chemistry related anyway question
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Q2. Organic inorganic physical
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Q3. Coordination chemistry organometallic chemistry
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Q4. Organic chemistry
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Q5. Physical chemistry
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Knowledge about DRA and skills

DRA. Case study about current situation.

Q1. What is meaning off Gmp
Ans. Gmp is part of Quality assurance which is ensure that the product are consistently produce with precautions of Quality and safety
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Q2. What meaning of current good manufacturing practices
Ans. Current good manufacturing practices means it is process adopted by the manufacturing which proves to be nessesary and important of ,identity,strengh,purity of api production
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Q1. About IPQA, PROCESS VALIDATION
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Q2. About CPP,CQA, Coating
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Q1. General Introduction
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Q2. Discussion About study of pharma and subjects
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Q1. Basic of pharma and industrial training and experience
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Q2. General of pharmacutical and tablet dosage form
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