Welcome to the critical world of Pharmacovigilance, where patient safety meets drug development.
Are you gearing up for an interview in this vital field? Wondering what questions might come your way? In this video, we’ll guide you through the most common interview questions and arm you with insightful answers that could set you apart. From adverse drug reactions to post-marketing surveillance, we’ve got your preparation covered. So, stay tuned as we delve into the essentials of Pharmacovigilance interviews, right here on our channel
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Links Monitoring visit Series -
Adverse Events & Adverse Drug Reaction: [ Ссылка ]
Serious Adverse Events: [ Ссылка ]
Phases of Clinical Trials: [ Ссылка ]
Links to most helpful videos:
CRA Interview: [ Ссылка ]
CRC interview: [ Ссылка ]
Clinical Research Coordinator: [ Ссылка ]
Clinical Research explained under 5 mins: [ Ссылка ]
13 Principle of ICH-GCP: [ Ссылка ]
CRC or CRA: [ Ссылка ]
Phases of Clinical trials: [ Ссылка ]
Good Clinical Practices (ICH-GCP): [ Ссылка ]
Ethics Committee in Clinical Research: [ Ссылка ]
NDCT Rules 2019: [ Ссылка ]
SAE reporting and SUGAM: [ Ссылка ]
Adverse events (AE) in Clinical Trials: [ Ссылка ]
For queries about Advanced Certification in Clinical Research, please reach out/contact at below mentioned platforms
Contact: +91 77219 76079 / 83900 88032
To Register, please click on the link below:
[ Ссылка ]
Instagram ID: clinical_aim_research
Gmail: clinicalaimresearch@gmail.com
For any queries, kindly comment in the description box below.
In this video, We explain about:
(0:00) Intro
(1:22) What is Pharmacovigilance?
(3:98) Interview Q&A
(11:41) Position & Salary
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