Master Pharmaceutical Products Registration in Oman
Get a great market share of Sultanate of Oman for pharmaceutical products
Updated on Sep, 2023
Language - English
Course Description
Master pharmaceutical products registration in one of the most interesting parts of the GCC countries, quite big virgin market, full of opportunities, let's grape this huge opportunity and place our pharmaceutical products there in the market of Oman.
In this course, I will take you on such an interesting journey with the Ministry of the health of Oman, to master our pharmaceutical products registration there, let's practice regulatory affairs, registration, renewal, variations with all its stypes, classification, case by case using actual examples from practice. As I always keep my theme in the pharma academy that "It comes to you from practice"
The market of Oman is quite virgin compared to other GCC markets, which are actually saturated with most of the kinds of products, such as the leader of the region "KSA" and the gulf region business hup "UAE", which means there is a huge opportunity waiting for us there, to master the market and have quite a big market share with our pharmaceutical products, and do not forget about the tenders, they are basic market players in all GCC countries markets.
In this course, we will cover all topics related to pharmaceutical products in Oman, that will empower you to master the market. Then we will go deeper to see the actual forms, and templates as usual I keep the theme of the Pharma Academy that it comes to you "From Practice", and prepare the submission dossier together, and ensure its verification, and interact with the actual system for the submission.
we will end our journey, by landing the department of custom clearance, tracking /tracing system, barcoding, 2DMatrix for all the shipments planned for Oman market importation.
The system which was first implemented by KSA the leader of the region, and then Oman, UAE, Bahrain followed so far, and the others are coming soon.
And finally, congratulations to you for mastering medical device registration in the Oman market, and see you soon in the pharma industry my dear colleagues.
See you onboard
Let's take-off
Who this course is for:
- All levels of the pharma industry, starting from the fresh graduates till the highly professionals
Goals
What will you learn in this course:
Master pharmaceutical products registration in Sultanate of Oman
Manage pharmaceuticals regulatory pathway in Sultanate of Oman
Get a market share in Sultanate of Oman market
Place your pharmaceutical products in Sultanate of Oman market
Prerequisites
What are the prerequisites for this course?
Just the PC and welling to stand out of the crowd
Curriculum
Check out the detailed breakdown of what’s inside the course
Master Pharmaceutical Products Registration in Oman
12 Lectures
-
Introduction
14:35
14:35
-
Transition to the eCTD
09:58
09:58
-
Module 1
09:14
09:14
-
Core eCTD
12:55
12:55
-
Dossier Evaluation
22:11
22:11
-
Validation/Renewal/Variation
06:59
06:59
-
M1 eCTD preparation
18:51
18:51
-
Country specific elements
06:08
06:08
-
M1 electronic submission
20:59
20:59
-
Actual Forms
39:10
39:10
-
ECTD Renewals/Variations
16:58
16:58
-
Barcoding/Closing
13:38
13:38
Instructor Details
Zahra Hassan Sobhy
This is Zahra Hassan, I'm a pharmacist, with almost 10 years of experience in the pharma industry, my experience is extended to cover the regulatory affairs field, which deals with registration and granting health authorities approval for health products, including medicines, medical devices, over the counter products "OTC", such as food supplements, and cosmetics as well.
This is in addition to the quality compliance, control, and assurance for these health products, and also ensuring product safety through pharmacovigilance activities.
I have been practicing all these professions for 10 years covering 20 countries, across the regions of the Middle East, Africa, Levant, and Turkey.
During my career journey, I gave myself lots of credits by postgraduates studies
Msc of pharmacovigilance Bordeaux university France
MBA, Chiffley buisneiss school , Australia
Dual Diploma of regulatory affairs "pharmaceutical and medical devices" RAP society, USA.
Certified lead auditor
currently enrolled in the Ph.D. program of pharmacovigilance Bordeaux university France
Despite the fact that postgraduate studies for sure will add to the profile, but the practice is something else, in the begging of my career journey I was chasing professionals asking for private lessons after work to gain practical experience from them, and it was not for free, I used to make this deal with many professionals as I can to get as much diverse experience that I can gain, in addition, I used to follow national and international pharma industry events attending, then participating from my own pocket. This simply happens when you follow your passion.
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