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
https://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 mypharmacareer2@gmail.com
Watch our this video for more details
https://youtu.be/IkeKKXRtrdI
E book needed
Exiting news-Now you get 50% off on eBook-An introduction to Drug Regulatory affairs
Now purchase book for only 199/- for limited period
Here is a link to purchase
https://thingsbyamit.stores.instamojo.com/product/849281/introduction-to-drug-regulatory-affairs?sideBar=setup&view=desktop
Sir, will you send the book to us on email id?
Thanks Amit sir
Thank you for this great knowledge.
Hello Sir, regulary affairs and medical writing me konsa preffer karna chahiye... And abroad job ke liye kaha jada scope he.. Medical writing or RA? Please guide
Sir again request u plz make vedio on msc clinical biochemistry after bsc ...it's scope and job opportunities
Please update in English
Sir b pharmacy complete hone ki baad koun se department mi job karna chahiye and best Appertunty ho , best sallery ho and foreign jaane ka
Sir ji best department konsa rahega pharmacovigilance ya regularity affairs plz tell me
Hi,
Please made vedio on how to apply job so that can be reached more and more to recruiters and HR for interview call.
Swati pal
Fresher
Ready to relocate
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
https://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 mypharmacareer2@gmail.com
Watch our this video for more details
https://youtu.be/IkeKKXRtrdI
Sir, can you plz tell me, Does post graduation diploma in RA affect my b. Pharm degree??? Plz tell me
Hello sir
I have done my masters in chemistry in India and now i am planning for further study in Canada. And i am thinking for regulatory affair course which is a PG diploma course. So can you tell me what are the chances for getting field job after regulatory affairs ?
How is the scope in Canada for regulatory affairs ?
Please answer me sir 🙏
Sir I have done bachelors in Biochemistry and I have 2 yrs experience in IVD industry as production chemist Can i go for regulatory affairs..
Which skill need before going in Regulatory affairs department ?
Ctd common technical document..it is
B.pharm vale bhi bhi RA me ja skte h ya m.pharm Valo Ke liye Jada preferable hota h ye??
Sir I'm m pharm (quality assurance) can have any chance to get job in regulatory affairs
Most company hire phrma students for RA .
Will it be difficult for MSc student to get job selection for regulatory affairs as compare pharma students ?
I have done my MSc chemistry can I do job in regulatory affairs ?
Which field is better in this?
RA or PV
Pharmacovgilence or drug regulatory affairs kon job easy se mil jati hai plz
How is scope after regulatory affairs course in usa and what will be the avg salary in us
Sir can a bds apply for it?
Is it good career to me please let me know
Sir i hv done Mpharm pharmacy practice and i got job in RA
Class kuthe ahe Ra chr
Sir, please reply.
Can indians get job in drug regulatory affairs in canada or usa???
After b pharm or m pharm in DRA.
Hello Sir, I am a B.pharm graduate and working as a fresher in RA industry. I want to pursue my career in RS only. Should I go for PG diploma in RA, is it well accepted by the industry??
After mpharma can we do this RA course ??
As it is difficult to find job
for cracking the interview of regulatory affairs may I need to prepare the therapeutic
drug classification
Sir agar m pharm kisii bhi private toh uska koi scope hota hai ya nahi
thank you Sir🙏
I'm going to attend interview for Regulatory affairs, but i did msc chemistry and i don't have much knowledge abut RA.Most of the companies hire m.pharma students it seems...will it become problem in future if i strt career in RA??
Please suggest institute for PG diploma and certification course for Regulatory Affairs.
is PG-diploma enough to get a job and growth in Regulatory affairs
Wow❤🥰
Really interesting bcuz study completed from Bhopal me also💕
Am doing M.pharm in regulatory affairs. so where is my best scope ?
Which university college is best for b pharmacy in placements please please tell me
Hi Mam. I am a Msc Biotechnology student so can i do internship on GRA (REG AFFAIRS)? What do u have to tell about the scope?
Please do respond to my query 💖
Neha mam, did diploma in regulatory course, where, and if campus selection does not take place
Sir can you plz upload other interview videos this can help us very much
Is it worth having m.pharm in dra?
Such a great interview! She spoke out of her heart. Thank you so much, please continue this series to inspire more and more pharma students.
I completed m pharmacy in pharmaceutical regulatory affairs, and I have one year experience in medical device in first data bank, but i unable to understand we should I start my career? Help me regarding this, and l don't want to go pharma industry
Academic study and industry me bahut bada gap bana huaa hai faculty industry ke hisab se update nahi hai faculty ko applied knowledge nahi hai sedantik knowledge se kaam nahi chalega
Very well said didi👍👍👍
Very good Presentation
Very very congratulations dear neha beta.we proud of you.
Keep it up Neha, you made us proud
Wow Neha didi
Thank you so much Sir 🙏😊
Sir part 2 nhi mila 🤔?
Itna slow speed hai ki mood off ho ja rha haj
sir second section kaha h link
Please suggest me for DI preparation book
Thank you so much sir
👍 sir please GPAT ke exam ke liye bhi lecture series banaye
Thanks for information,could u tell me any book related in vaccine prepartion(Biotechpharma).
Good > Great > greatest
Slides and presentation is top class. Best combination of colour with book orange book and always best teaching
Nice
Thank u
Very useful topic sir..as I finding in regulatory affairs and I find such great information
RRB 2019 me question aya tha ispe👍