Updated interview questions asked in Interview of Drug Regulatory Affairs

[@ThingsbyAmit]

Hello everyone Happy to announce we first time announce 3 month Certificate course in Drug regulatory Affairs Batch1 which is India’s most affordable course. Here are details of course Topics covered Fundamentals of Drug Regulatory Affairs Class 1 i)ntroduction ii)Definition, Rationale, iii)Roles and responsibilities Class 2 i)How Regulatory Affairs works in Pharmaceutical Company ii)Different Regulatory Authorities Class 3 i)Innovator and Generic Drugs ii) Drug development process Class 4 i)Different guidelines used in Regulatory work. Class 5 i) ICH Guidelines In depth Quality guidelines and Overview of Safety, Efficacy and Multidisciplinary guidelines ii)WHO guideline Class 6 CTD Structure In depth Module wise content detailing Class 7 i)ACTD Structure In depth Part wise content detailing ii) Difference between CTD and ACTD Class 8 Dossier filing process for Europe, USA and Rest of world market Class 9 Different types of documents required for Dossier preparation and their explanation Class 10 Post approval process: Variations and Renewals Class 11 Overview of Clinical Trials and their phases, Pharmacovigilance, PSUR Class 12 Frequently asked interview questions with answers Timing for Webinar 3 pm to 5 pm (2 hours weekly on Sunday) All classes are virtual through Zoho Course will starts from 27 March till 16 June Benefits 1)You will get certificate from ISO certified organization 2)You will get lifetime free counselling from our side 3)Recorded lectures 4)swot analysis,mock interview,skill improvement Who can ENROLL Anyone who wish to learn Pharmacovigilance from science background How to enroll Course fee-3999/- Early bird registration Offer price -2999/- till 20 March 2022 Click following link to enroll rzp.io/l/USHzct3Ll5 OR Pay online (Gpay/Phonepay/Paytm) to 9423272876 After payment share screenshot to 9423272876 via whatsup After payment from any above mentioned way you will get confirmation email with seat allotment You will be added to Whatsup group one day prior to Class 1 All admissions opens till 26 March or up to seats fulfilment whichever earliest If any query you can mail at [e-mail] Watch our this video for more details kzbin.info/www/bejne/f5zIfH6Oh9mlmqs

[@sanjananaik1783]

This will be more helpful to all... Who are preparing for interviews 🙏

[@piscesperfectionist]

Thanks for the valuable information

[@pravingore6152]

Well explained.. please share this type of videos

[@krish_krish354]

Thank you for ur details about regulatory works🙏

[@sanjananaik1783]

Sir aise he videos banaye plz 🙏

[@patilpinal9081]

Thank u well explained

[@onkarjoshi4735]

thnax amit it is very nice video

[@pratiksonawane3851]

Thanks👍

[@meenac]

thank you and please tell detailed abt mutual ,decentralized, national, nonmutual procedures for europe

[@ThingsbyAmit]

That will be covered in our certificate course in Drug regulatory affairs

[@meenac]

@@ThingsbyAmit detailed matter not there na sir?

[@Harshaledits...]

Nice information 👌🏻

[@bantysharma1508]

Q 7 is not answer properly and all is good.

[@krish_krish354]

After 3 yrs one application submit what is that sunset clause or cloud application? 6.09 min

[@payellaha2748]

Sunset Clause application

[@shivamsanap8439]

Helpful

[@tusharpatil679]

Which type of education is important for regularly affairs

[@hemalivaghela6315]

B.pharm and m.pharma in RA

[@tusharpatil679]

Hi

[@abhishekpednekar8468]

Nice

[@tusharpatil679]

I mean mpharm ,msc

[@ThingsbyAmit]

M pharmacy