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10+ Anuj Goyal Associates Interview Questions and Answers
Q1. What do you know about PV? What's are health authority in the World? Normal basic PV questions which you can find Google
Pharmacovigilance (PV) is the science of detecting, assessing, and preventing adverse effects of drugs.
PV is responsible for monitoring the safety of drugs and ensuring that the benefits outweigh the risks.
PV involves collecting and analyzing data on adverse drug reactions (ADRs) and other drug-related problems.
PV is important for ensuring patient safety and improving public health.
Health authorities in the world include the FDA (USA), EMA (Europe), MHRA (UK), TGA (Australia)...read more
Q2. What's ICSR, Susar and other things!
ICSR is Individual Case Safety Report and SUSAR is Suspected Unexpected Serious Adverse Reaction.
ICSR is a report of an adverse event or reaction that occurs in an individual patient.
SUSAR is an adverse reaction that is both unexpected and serious.
Pharmacovigilance associates are responsible for collecting and analyzing ICSRs to ensure drug safety.
Other important terms in pharmacovigilance include ADR (adverse drug reaction), SAE (serious adverse event), and CIOMS (Council fo...read more
Q3. Difference between AE and SAE
AE stands for Adverse Event and SAE stands for Serious Adverse Event.
AE refers to any untoward medical occurrence in a patient or clinical trial subject, which does not necessarily have a causal relationship with the treatment being administered.
SAE refers to any untoward medical occurrence that results in death, is life-threatening, requires hospitalization or prolongation of existing hospitalization, results in persistent or significant disability/incapacity, or is a congen...read more
Q4. explain medical coding how u choose for exact ADR
Medical coding is the process of assigning standardized codes to medical diagnoses and procedures to ensure accurate reporting and billing.
Medical coding involves using standardized code sets such as ICD-10, CPT, and HCPCS.
To choose the exact adverse drug reaction (ADR) code, pharmacovigilance associates need to carefully review the patient's medical records, laboratory results, and any other relevant information.
The ADR code chosen should accurately reflect the specific adve...read more
Q5. What is pharmacovigilance . How far do you live ? Can you work in shift basis ?
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 the safety of pharmaceutical products after they have been released to the market.
It includes collecting and analyzing data on adverse drug reactions and other drug-related problems.
The goal of pharmacovigilance is to improve patient safety and minimize risks associated w...read more
Q6. TYPES OF ADR discription of how to attend RA
Types of Adverse Drug Reactions (ADRs) and how to attend Regulatory Authorities (RA)
Types of ADRs include Type A (predictable, dose-dependent), Type B (idiosyncratic, not dose-dependent), Type C (chronic), Type D (delayed), and Type E (end-of-treatment)
To attend Regulatory Authorities (RA) regarding ADRs, report all suspected adverse reactions promptly and accurately
Provide detailed information such as patient demographics, medical history, concomitant medications, and descri...read more
Q7. Explain digestion
Digestion is the process of breaking down food into smaller molecules that can be absorbed by the body.
Digestion starts in the mouth where food is chewed and mixed with saliva.
The food then travels down the esophagus into the stomach where it is further broken down by stomach acid and enzymes.
In the small intestine, nutrients are absorbed into the bloodstream.
The remaining waste moves into the large intestine where water is absorbed and the waste is formed into feces.
Finally,...read more
Q8. What is future opinion
Future opinion refers to the anticipated views or beliefs that individuals may hold in the future.
Future opinion can be influenced by various factors such as advancements in technology, changes in societal norms, and evolving scientific research.
It is important for pharmacovigilance associates to consider future opinions when assessing the safety and efficacy of pharmaceutical products.
For example, a drug that is currently considered safe may face backlash in the future due t...read more
Q9. what is pharmacovigilance
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 the safety of medications after they have been approved and marketed.
It includes collecting and analyzing data on adverse drug reactions and other drug-related problems.
Pharmacovigilance aims to improve patient safety and minimize risks associated with medication use.
Exam...read more
Q10. Where are you form
I am from New York City, USA.
I was born and raised in New York City.
I have lived in the USA my whole life.
I am familiar with the healthcare system in the US.
Q11. Role of pharmacovigilance
Pharmacovigilance involves monitoring, evaluating, and preventing adverse effects of pharmaceutical products.
Monitoring and reporting adverse drug reactions
Evaluating the safety profile of drugs
Identifying and assessing risks associated with medications
Preventing harm to patients by ensuring safe use of drugs
Regulatory compliance and reporting to health authorities
Continuous monitoring of drug safety post-marketing
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