Announcing ‘3 months online certification course in drug regulatory affairs’ batch 6
Hello all
In this video we announce’3 months online certification course in drug regulatory affairs’ batch 6
To watch demo class click here
Demo class for Drug Regulatory course
https://youtu.be/MEdkcuA_7Io
fill this googleform for any query
https://docs.google.com/forms/d/e/1FAIpQLScspRbBJMEx9pmlFvd-b4pUOsWhYF7uNnrJ4X-CzGXjZh83Pg/viewform?usp=sf_link
For inquiry and enrolment about ‘3 months online certification course in drug regulatory affairs’ from our academy ’Global Pharma Academy ’kindly fill this googleform
https://docs.google.com/forms/d/e/1FAIpQLScspRbBJMEx9pmlFvd-b4pUOsWhYF7uNnrJ4X-CzGXjZh83Pg/viewform?usp=sf_link
Here are details of course
Happy to announce we announce 3 month Certificate course in Drug regulatory Affairs Batch 6 which is India’s most affordable course.
Topics covered
Class 1
i)Introduction
ii)Definition, Rationale, iii)Roles and responsibilities
Class 2
i)How Regulatory Affairs works in Pharmaceutical Company
ii)Different Regulatory Authorities
iii)Innovator and Generic Drugs
iv) Drug development process
Class 3
i)Different guidelines used in Regulatory work.
Class 4
i) ICH Guidelines
In depth Quality guidelines and Overview of Safety, Efficacy and Multidisciplinary guidelines
Class 5
CTD Structure
In depth Module wise content detailing
Class 6
i)ACTD Structure
In depth Part wise content detailing
ii) Difference between CTD and ACTD
Class 7
Dossier filing process for Europe, USA and Rest of world market
Class 8
Different types of documents required for Dossier preparation and their explanation
Class 9
Post approval process: Variations and Renewals
class 10
Overview of medical device regulatory
Class 11
Overview of Clinical Trials and their phases, Pharmacovigilance, PSUR
Class 12
Frequently asked interview questions with answers
Timing for class
1 pm to 3pm (2 hours weekly on Sunday)
All classes are virtual through Zoho
Course will starts from 26 November 2023 onwards
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 Drug Regulatory Affairs from science background
Fees -8999/-
How to enrol
click here
https://rzp.io/l/TyttWqhr7R
Pay online via 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.
You will be added to Whatsup group one day prior to Class 1
All admissions opens till seats fulfilment (40)
If any query email us at mypharmacareer2@gmail.com
#drug regulatory affairs certification course
Видео Announcing ‘3 months online certification course in drug regulatory affairs’ batch 6 канала Things by Amit
In this video we announce’3 months online certification course in drug regulatory affairs’ batch 6
To watch demo class click here
Demo class for Drug Regulatory course
https://youtu.be/MEdkcuA_7Io
fill this googleform for any query
https://docs.google.com/forms/d/e/1FAIpQLScspRbBJMEx9pmlFvd-b4pUOsWhYF7uNnrJ4X-CzGXjZh83Pg/viewform?usp=sf_link
For inquiry and enrolment about ‘3 months online certification course in drug regulatory affairs’ from our academy ’Global Pharma Academy ’kindly fill this googleform
https://docs.google.com/forms/d/e/1FAIpQLScspRbBJMEx9pmlFvd-b4pUOsWhYF7uNnrJ4X-CzGXjZh83Pg/viewform?usp=sf_link
Here are details of course
Happy to announce we announce 3 month Certificate course in Drug regulatory Affairs Batch 6 which is India’s most affordable course.
Topics covered
Class 1
i)Introduction
ii)Definition, Rationale, iii)Roles and responsibilities
Class 2
i)How Regulatory Affairs works in Pharmaceutical Company
ii)Different Regulatory Authorities
iii)Innovator and Generic Drugs
iv) Drug development process
Class 3
i)Different guidelines used in Regulatory work.
Class 4
i) ICH Guidelines
In depth Quality guidelines and Overview of Safety, Efficacy and Multidisciplinary guidelines
Class 5
CTD Structure
In depth Module wise content detailing
Class 6
i)ACTD Structure
In depth Part wise content detailing
ii) Difference between CTD and ACTD
Class 7
Dossier filing process for Europe, USA and Rest of world market
Class 8
Different types of documents required for Dossier preparation and their explanation
Class 9
Post approval process: Variations and Renewals
class 10
Overview of medical device regulatory
Class 11
Overview of Clinical Trials and their phases, Pharmacovigilance, PSUR
Class 12
Frequently asked interview questions with answers
Timing for class
1 pm to 3pm (2 hours weekly on Sunday)
All classes are virtual through Zoho
Course will starts from 26 November 2023 onwards
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 Drug Regulatory Affairs from science background
Fees -8999/-
How to enrol
click here
https://rzp.io/l/TyttWqhr7R
Pay online via 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.
You will be added to Whatsup group one day prior to Class 1
All admissions opens till seats fulfilment (40)
If any query email us at mypharmacareer2@gmail.com
#drug regulatory affairs certification course
Видео Announcing ‘3 months online certification course in drug regulatory affairs’ batch 6 канала Things by Amit
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