Master Medical Devices Registration in Oman
Manage regulatory pathway of medical devices in Oman
Business,Industry,Medical Device Development
Lectures -8
Resources -11
Duration -2 hours
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Course Description
Master medical devices 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 medical devices 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 medical devices 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, 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 GCC 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 Oman market.
In this course, we will cover all topics related to medical devices 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, 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, 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.
Goals
Master medical devices registration in Oman
Manage regulatory affairs practising in Oman
Place your medical devices in Oman
Manage the whole regulatory pathway of medical devices in Oman
Prerequisites
Just the PC and welling to stand out of the crowd
Curriculum
Check out the detailed breakdown of what’s inside the course
Master Medical Devices Registration in Oman
8 Lectures
- Introduction 20:14 20:14
- Classification Jurisdiction 08:44 08:44
- The application form 22:03 22:03
- The dossier submission 13:23 13:23
- The Checklist 12:39 12:39
- Listing of medical devices 28:19 28:19
- Variations 29:56 29:56
- Tracking/Tracing System 05:54 05:54
Instructor Details
Zahra Hassan Sobhy
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