Master pharmaceutical products registration in the Levant
Master pharmaceutical products registration in Lebanon nd Syria
Updated on Sep, 2023
Language - English
Master pharmaceutical products registration in the levant, the part of the world driven by Jordan from a regulatory point of view, as both Lebanon and Syria are following JFDA of Jordan for the regulation of both medical devices and pharmaceutical products, and consequently JFDA is following SFDA of Saudi Arabia.
So in this quick journey, we will explore the regulations of pharmaceutical products in both Lebanon and Syria
We will manage to place our pharmaceutical products in Lebanon and Syria of the Levant area
We will compare the regulatory pathway of pharmaceutical products in both Lebanon and Syria, due to many similarities, however, Jordan has its own course titled "Pharmaceutical products registration in Jordan" due to many details , updates and the course is so long, cannot be added here, in addition to that JFDA has its won regulations which are so advanced compared to either Lebanon or Syria regulations, besides that JFDA adopted the eCTD system for the submission of pharmaceutical products with its own implemented Module 1, however, both Lebanon and Syria still the process of dossier submission is through the paperwork.
In the last section of our course, we will explore the latest updates of the Lebanon ministry of health regarding pharmaceutical products registration following the updates that were implemented previously in the GCC.
See you onboard
Who this course is for:
- All levels of Pharma student , fresh graduates, and Pharma industry professionals
What will you learn in this course:
- Master pharmaceutical products registration in the Levant
- Master pharmaceutical products registration in Lebanon and Syria
- Place your pharmaceutical products in the Levant
- Place your pharmaceutical products in Lebanon and Syria
What are the prerequisites for this course?
Just laptop and willing to learn to stand out of the crowd
Check out the detailed breakdown of what’s inside the course
- Introduction 14:17 14:17
Lebanon Pharmaceutical Regulations
Pharmaceutical Products Submission
Syria Pharmaceutical Products Registration
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.
User your certification to make a career change or to advance in your current career. Salaries are among the highest in the world.
Our students work
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