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10+ Sri Taralabalu Jagadguru Residential School Interview Questions and Answers

Updated 15 Oct 2024
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Q1. what is the difference between product abuse and misuse

Ans.

Product abuse is intentional misuse of a product, while product misuse is unintentional or accidental use of a product.

  • Product abuse is a deliberate act of using a product in a way that is not intended or recommended, often for recreational purposes or to achieve a high.

  • Product misuse, on the other hand, is the unintentional or accidental use of a product in a way that is not recommended or intended.

  • Examples of product abuse include using prescription drugs recreationally, us...read more

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Q2. what is the difference between adverse event and reaction?

Ans.

Adverse event refers to any undesirable medical occurrence, while reaction is a specific response to a drug or medical intervention.

  • Adverse event is a broader term that encompasses any negative medical occurrence, whether or not it is related to a drug or medical intervention.

  • Reaction specifically refers to a response to a drug or medical intervention.

  • Adverse events can include things like falls, infections, or other medical issues that may or may not be related to a drug or ...read more

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Q3. What is the difference between clinical research and pharmacovigilance.

Ans.

Clinical research involves testing new drugs or treatments on humans, while pharmacovigilance involves monitoring the safety of drugs already on the market.

  • Clinical research is conducted during drug development to determine safety and efficacy.

  • Pharmacovigilance involves monitoring the safety of drugs already on the market and identifying adverse reactions.

  • Clinical research is typically conducted in a controlled environment, while pharmacovigilance relies on real-world data.

  • Cl...read more

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Q4. what are the basic requirements in a case

Ans.

The basic requirements in a case are essential elements or conditions that must be met for the case to proceed.

  • Clear and concise facts

  • Relevant evidence

  • Applicable laws and regulations

  • Proper documentation

  • Objective analysis

  • Logical reasoning

  • Effective communication

  • Timely resolution

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Discover Sri Taralabalu Jagadguru Residential School interview dos and don'ts from real experiences

Q5. What is Pharmacovigilance. What is MeDraw. Explain anything about Argus.

Ans.

Pharmacovigilance is the science and activities related to the detection, assessment, understanding, and prevention of adverse effects or any other drug-related problems.

  • Pharmacovigilance is important for ensuring the safety of drugs and protecting public health.

  • It involves monitoring and analyzing data from various sources, including clinical trials, spontaneous reports, and literature.

  • MeDraw is not a known term in pharmacovigilance.

  • Argus is a pharmacovigilance software deve...read more

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Q6. what are the types of clinical trials

Ans.

There are four types of clinical trials: Phase I, Phase II, Phase III, and Phase IV.

  • Phase I trials test the safety and dosage of a new drug on a small group of healthy volunteers.

  • Phase II trials test the effectiveness and side effects of a new drug on a larger group of patients with the targeted disease.

  • Phase III trials compare the new drug to the current standard treatment on a large group of patients to determine its safety and effectiveness.

  • Phase IV trials are conducted af...read more

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Q7. what is pharmacovigilance

Ans.

Pharmacovigilance is the science and activities related to the detection, assessment, understanding, and prevention of adverse effects or any other drug-related problems.

  • Pharmacovigilance involves monitoring and evaluating the safety of pharmaceutical products.

  • It aims to identify and assess adverse drug reactions (ADRs) and other drug-related issues.

  • Pharmacovigilance activities include collecting and analyzing data from healthcare professionals, patients, and regulatory autho...read more

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Q8. Difference between Adverse event and adverse effect.

Ans.

Adverse event is any undesirable experience associated with the use of a medical product. Adverse effect is a harmful and unintended reaction to a medical product.

  • Adverse event refers to any negative experience that occurs during the use of a medical product, regardless of whether it is related to the product or not.

  • Adverse effect refers specifically to a harmful and unintended reaction to a medical product.

  • Adverse events can include things like nausea, headache, or dizziness...read more

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Q9. Difference between AE and ADR

Ans.

AE refers to any untoward medical occurrence in a patient, while ADR specifically refers to a harmful and unintended reaction to a medication.

  • AE can include symptoms, signs, diseases, or worsening of pre-existing conditions, while ADR is a subset of AE caused by a medication.

  • AE can be expected or unexpected, while ADR is always unexpected.

  • Examples of AEs include headache, nausea, or fever, while examples of ADRs include drug-induced liver injury or anaphylaxis.

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Q10. Explain labelling

Ans.

Labelling refers to the information provided on a product's packaging or container.

  • Labelling includes important information such as dosage instructions, warnings, and ingredients.

  • In the medical field, labelling is particularly important for ensuring patient safety and proper use of medications.

  • Examples of labelled products include prescription medications, over-the-counter drugs, and food packaging.

  • Labelling requirements may vary by country or region, and are often regulated ...read more

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Interview Process at Sri Taralabalu Jagadguru Residential School

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3 Interview rounds
Resume Shortlist Round
HR Round
Personal Interview1 Round
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