Master Medical Devices, Pharma Products Registration Tunisia
Manage all regulatory activities for both medical devices, and pharmaceutical products in Tunisia
Updated on Sep, 2023
Language - English
Course Description
Master both medical devices and pharmaceutical products registration in one of the most interesting parts of Africa, the huge market there full of opportunities, let's grape the opportunity and place our medical devices there in the market of Tunisia.
In this course, I will take you on such an interesting journey with the Ministry of the health of Tunisia, to master our medical devices and pharmaceutical products registration there, let's practice regulatory affairs, registration, renewal, variations with all its types, 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 Tunisia is Huge compared to other markets of Africa, which means there is a huge opportunity waiting for us there, to master the market and have quite a big market share, especially with medical devices, due to the continuous innovations of the medical devices, and do not forget about the tenders, they are basic market players in all countries markets.
So from a business point of view, considering the registration timeframe between 6 to 9 months maximum, you can place your product in the market quite faster and start earning your revenue quite fast also, moreover, the medical devices world is highly dynamic and innovative, compared to the pharmaceuticals, lots of innovations different versions of the same medical device could be played within the potential market of Tunisia.
In this course, we will cover all topics related to medical devices, and pharmaceutical products in Tunisia, 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, budling /grouping criteria of the medical devices in only one application, and interact with the actual system for the submission
and we will end our journey, by landing the department of custom clearance, tracking /tracing system, barcoding, for all the shipments planned for Tunisian market importation.
And finally, congratulations to you for mastering medical device, and pharmaceutical products registration in the market of Tunisia, and see you soon in the pharma industry my dear colleagues.
Who this course is for:
- All levels of pharma industry professionals and fresh graduates
Goals
What will you learn in this course:
Master Medical devices, and pharmaceutical products registration in Tunisia
Manage all regulatory activities for both medical devices, and pharmaceutical products in Tunisia
Place your medical devices, and pharmaceutical products in the market of Tunisia
Master the medical devices, and pharmaceutical products market of Tunisia
Prerequisites
What are the prerequisites for this course?
Just a laptop and a desire to stand out of the crowd
Curriculum
Check out the detailed breakdown of what’s inside the course
Master Medical Devices, Pharma Products Registration Tunisia
9 Lectures
-
Introduction Medical Devices
07:43
07:43
-
Submission Dossier Medical Devices
03:12
03:12
-
Regulatory Process Medical Devices
03:02
03:02
-
Pharmacovigilance Medical Devices
04:31
04:31
-
Registration Guidelines Pharmaceuticals
12:10
12:10
-
Renewal Pharmaceutical products
04:11
04:11
-
Variations
07:57
07:57
-
Pharmacovigilance
16:16
16:16
-
Approvals
05:42
05:42
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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