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The latest version of MedDRA is version 24.1.
MedDRA stands for Medical Dictionary for Regulatory Activities.
It is a standardized medical terminology used for the classification of adverse event information associated with the use of pharmaceuticals.
Version 24.1 includes updates and additions to terms and codes for adverse events.
It is important for pharmacovigilance professionals to stay updated on the latest vers...
Timelines of non serious cases are typically shorter than serious cases, usually ranging from a few days to a few weeks.
Non serious cases usually have a quicker resolution compared to serious cases
Timelines can vary depending on the specific case and the actions taken by the pharmacovigilance team
Follow-up may be required to ensure the case is fully resolved
Examples: Mild allergic reactions, minor side effects lik...
Active participation during audit includes preparing for the audit, attending audit meetings, providing requested information, and addressing any findings or concerns.
Prepare for the audit by reviewing relevant documents and processes
Attend audit meetings and actively participate by answering questions and providing explanations
Provide requested information promptly and accurately
Address any findings or concerns r...
Communication in drug safety involves emails, phone calls, and meetings to ensure timely and accurate information exchange.
Emails are commonly used for formal communication and documentation of important information.
Phone calls are used for more immediate and urgent communication, such as discussing adverse events or safety concerns.
Meetings are held to facilitate discussions, decision-making, and collaboration am...
Precautions and improvisations for improving data management in drug safety
Implementing standardized data entry protocols to ensure consistency and accuracy
Regularly conducting data quality checks and audits to identify and correct errors
Utilizing advanced data management software and tools for efficient data processing
Ensuring data security and confidentiality measures are in place to protect sensitive informatio...
GVP guidelines ensure the safety and efficacy of medicinal products through effective pharmacovigilance practices.
GVP stands for Good Pharmacovigilance Practices, which are essential for monitoring drug safety.
It includes guidelines for reporting adverse drug reactions (ADRs) to regulatory authorities.
Example: A company must report any serious ADRs within 15 days of receiving the information.
GVP emphasizes the imp...
The OECD guidelines are a set of recommendations for policies and practices to promote economic growth and social well-being.
The OECD guidelines cover a wide range of topics including corporate governance, anti-corruption, environmental protection, and innovation.
They are designed to help governments, businesses, and individuals make informed decisions and improve their performance.
For example, the OECD guidelines...
I applied via Referral and was interviewed in Jun 2024. There was 1 interview round.
Active participation during audit includes preparing for the audit, attending audit meetings, providing requested information, and addressing any findings or concerns.
Prepare for the audit by reviewing relevant documents and processes
Attend audit meetings and actively participate by answering questions and providing explanations
Provide requested information promptly and accurately
Address any findings or concerns raised...
posted on 30 Aug 2024
I applied via Referral and was interviewed in Jul 2024. There was 1 interview round.
I appeared for an interview before Apr 2024, where I was asked the following questions.
I applied via Company Website and was interviewed in Mar 2023. There were 2 interview rounds.
I appeared for an interview before Mar 2024, where I was asked the following questions.
I applied via Referral and was interviewed before Oct 2023. There were 3 interview rounds.
Common aptitude test
Related to pharmacovigilance
I appeared for an interview before Feb 2024.
Report writing, annotating Excel, and grammatical correction.
I applied via LinkedIn and was interviewed before May 2023. There was 1 interview round.
The OECD guidelines are a set of recommendations for policies and practices to promote economic growth and social well-being.
The OECD guidelines cover a wide range of topics including corporate governance, anti-corruption, environmental protection, and innovation.
They are designed to help governments, businesses, and individuals make informed decisions and improve their performance.
For example, the OECD guidelines on c...
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The duration of ClinChoice interview process can vary, but typically it takes about less than 2 weeks to complete.
based on 15 interview experiences
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Bangalore / Bengaluru
4-8 Yrs
Not Disclosed
Senior Executive
54
salaries
| ₹4.3 L/yr - ₹12.1 L/yr |
Specialist
27
salaries
| ₹7.9 L/yr - ₹14 L/yr |
Executive Regulatory Affairs
22
salaries
| ₹3.2 L/yr - ₹5.8 L/yr |
Executive
18
salaries
| ₹3 L/yr - ₹5 L/yr |
System Engineer
14
salaries
| ₹3 L/yr - ₹4.5 L/yr |
IQVIA
Syngene International
SGS
Aragen Life Sciences