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Master Medical Devices Registration in Algeria

person icon Zahra Hassan Sobhy

4.4

Master Medical Devices Registration in Algeria

Manage all regulatory activities of medical devices in Algeria

updated on icon Updated on Jun, 2025

language icon Language - English

person icon Zahra Hassan Sobhy

English [CC]

category icon Business,Industry,Medical Device Development

Lectures -8

Resources -9

Duration -1.5 hours

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Course Description

Master medical device 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 Algeria.

In this course, I will take you on such an interesting journey with the Ministry of Health of Algeria to master our medical device registration there. Let's practice regulatory affairs, registration, renewal, and variations with all their types and classifications, 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 Algeria 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 and 9 months maximum, you can place your product in the market quite faster and start earning your revenue quite fast. Moreover, the medical devices world is highly dynamic and innovative; compared to the pharmaceuticals, lots of innovations and different versions of the same medical device could be played within the potential market of Algeria.

In this course, we will cover all topics related to medical devices in Algeria 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, bundling/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 customs clearance, tracking/tracing system, and barcoding, for all the shipments planned for Algerian market importation.

And finally, congratulations to you for mastering medical device registration in the market of Algeria, 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

  • Master Medical devices registration in Algeria

  • Manage all regulatory activities of medical devices in Algeria

  • Place your medical devices in the market of Algeria

  • Master the medical devices market of Algeria

Prerequisites

  • Just a laptop and a desire to stand out of the crowd

Master Medical Devices Registration in Algeria

Curriculum

Check out the detailed breakdown of what’s inside the course

Master Medical Devices Registration in Algeria

8 Lectures
  • play icon Introduction 10:45 10:45
  • play icon Actual Registration Process 09:50 09:50
  • play icon Classification 15:32 15:32
  • play icon Submission Forms 11:18 11:18
  • play icon Dossier Submission 14:23 14:23
  • play icon Attached Documents 13:46 13:46
  • play icon Dossier Evaluation and Acceptance 14:19 14:19
  • play icon Annual Importation Program 19:07 19:07

Instructor Details

Zahra Hassan Sobhy

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 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.

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