Pharmaceutical Products Registration United Arab Emirates
Be the expert of placing pharmaceutical products in the high potential market of the United Arab Emirates, business hub
Business,Industry,Medical Device Development
Lectures -18
Resources -29
Duration -4.5 hours
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Course Description
This course will prepare you, to be an expert in pharmaceutical products placement in the high potential market of the United Arab Emirates. the business hub of the Middle East region.
This course will provide you, with all tools that you need to run all regulatory activities related to the pharmaceutical products starting from the registration, to place these pharmaceutical products in the high potential diverse market of the UAE, in Dubai, the GCC region business hub.
Then to perform post-market placement activities, such as renewal/Checklist/Application and variations “Major/Minor”
and variations appendices, in addition to pharmacovigilance.
We will take off together to the United Arab Emirates together, starting our journey with the classification, as the basic mandatory step for the regulation of any product ever with any health authority ever. as they do not follow blindly the COO classification.
Goals
In this course you will master pharmaceutical products registration in the United Arab Emirates, the business hub of the Middle East in "Dubai".
You will manage all regulatory activities related to the Pharmaceutical products in the high potential market of the United Arab Emirates
You will be the expert to register, renew and make variations also to the Pharmaceutical products in the United Arab Emirates
You will place your Pharmaceutical products in the business hub of the Middle Est region , in the United Arab Emirates, in "Dubai"
Prerequisites
Just laptop and willing to succeed

Curriculum
Check out the detailed breakdown of what’s inside the course
Pharmaceutical Products Registration United Arab Emirates
18 Lectures
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Introduction 22:13 22:13
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LOA 06:47 06:47
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E-CTD 14:00 14:00
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M1 08:15 08:15
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MOHAP e-Transformation 12:10 12:10
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Attachments 11:41 11:41
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The Renewal 24:22 24:22
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Actual Applications 14:52 14:52
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Variations 16:48 16:48
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The Required Actions 32:12 32:12
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The Appendices 14:52 14:52
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Minor Variation 01:07 01:07
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Types of Variations 12:47 12:47
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Minor Variation Lists 22:04 22:04
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Minor Variation List Continue 20:06 20:06
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Variation Forms 12:13 12:13
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Tracking & Tracing 23:44 23:44
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The Updates 07:46 07:46
Instructor Details

Zahra Hassan Sobhy
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 through postgraduate 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 at Bordeaux University France
Even though postgraduate studies for sure will certainly add to the profile, the practice is something else, At the beginning 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 pocket. This simply happens when you follow your passion.
Course Certificate
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