Master Medical Device Registration In Saudi Arabia
Master Medical Device Registration In Saudi Arabia, available at $19.99, has an average rating of 4.4, with 15 lectures, 11 quizzes, based on 22 reviews, and has 73 subscribers.
You will learn about By the end of this course you will master medical devices registration in Saudi Arabia, the biggest GCC market ever Medical Devices Registration in Saudi Arabia Medical Devices Registration in KSA Medical Devices Registration in the biggest market in the GCC Medical Devices Registration in the highest ROI market in the GCC This course is ideal for individuals who are All Pharma industry professionals, regulatory affairs professionals, and those who deiced to start their career in the pharma industry It is particularly useful for All Pharma industry professionals, regulatory affairs professionals, and those who deiced to start their career in the pharma industry.
Enroll now: Master Medical Device Registration In Saudi Arabia
Summary
Title: Master Medical Device Registration In Saudi Arabia
Price: $19.99
Average Rating: 4.4
Number of Lectures: 15
Number of Quizzes: 11
Number of Published Lectures: 15
Number of Published Quizzes: 11
Number of Curriculum Items: 26
Number of Published Curriculum Objects: 26
Original Price: $129.99
Quality Status: approved
Status: Live
What You Will Learn
- By the end of this course you will master medical devices registration in Saudi Arabia, the biggest GCC market ever
- Medical Devices Registration in Saudi Arabia
- Medical Devices Registration in KSA
- Medical Devices Registration in the biggest market in the GCC
- Medical Devices Registration in the highest ROI market in the GCC
Who Should Attend
- All Pharma industry professionals, regulatory affairs professionals, and those who deiced to start their career in the pharma industry
Target Audiences
- All Pharma industry professionals, regulatory affairs professionals, and those who deiced to start their career in the pharma industry
Master medical devices registration in the most important and biggest market ever in the GCC region, the market of Sudi Arabia, this market could be missed by any pharmaceutical or healthcare company, all the pharma industry professionals understand very well the weight of this market, how huge it is, and what is the expected revenue out of it.
This course will equip you with two powerful tools to invade the pharma industry, as a regulatory affairs professional you are responsible for bringing up to 80% if not 90% of the company revenue from only one market in the GCC region in one hand while in your other hand you are dealing with the second powerful tool of the medical devices, as medical devices registration time frame is shorter than the pharmaceuticals, it is almost half the time frame of the pharmaceuticals.
To register a medical device you will need only 6 months, 3 months for variation, and 2 to 1 month only for renewal.
So from a business point of view, 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, with lots of innovations and different versions of the same medical device could be played within the potential market of the KSA.
Daer pharma industry future professionals, let us start our interesting journey towards medical device registration in KSA, we will travel together in Saudia Arabia, meet the health authority there “SFDA”, and explore its requirements for registration, renewal, and variations, let us get our MDMA and place our products there.
In this course, we will cover all topics related to medical devices in the KSA, starting from the requirements, interim regulations, classification, verification, and special conditions.
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 MDMA application, and interact with the actual SFDA gateway for MDMA submission.
and we will end our journey, by landing the department of custom clearance, tracking /tracing system, barcoding, and 2DMatrix for all the shipments planned for KSA market importation.
And finally, congratulations to you for mastering medical device registration in the KSA market, and see you soon in the pharma industry my dear colleagues.
Course Curriculum
Chapter 1: Introduction
Lecture 1: Introduction
Chapter 2: Medical Devices Classification
Lecture 1: Medical Devices Classification
Chapter 3: Medical Device Electronic System
Lecture 1: Medical Device Electronic System
Chapter 4: Guidance For Medical Devices Registration
Lecture 1: Guidance For Medical Devices Registration
Chapter 5: SFDA Submission Requirement
Lecture 1: SFDA Submission Requirements
Chapter 6: Notified Body
Lecture 1: Notified Body
Chapter 7: Classification
Lecture 1: Classification
Chapter 8: Registration Forms
Lecture 1: Registration Forms
Chapter 9: Templates
Lecture 1: Templates
Chapter 10: Bundling
Lecture 1: Bundling
Chapter 11: Bundling Diagrams
Lecture 1: Bundling Diagrams
Chapter 12: MDMA Application Process
Lecture 1: MDMA Application Process
Chapter 13: Verification
Lecture 1: Verification
Chapter 14: MDMA Certificate
Lecture 1: MDMA Certificate
Chapter 15: Clarence&PV
Lecture 1: Clearance &PV
Instructors
-
Dr. Zahra Hassan
Pharma industry expert
Rating Distribution
- 1 stars: 1 votes
- 2 stars: 1 votes
- 3 stars: 4 votes
- 4 stars: 4 votes
- 5 stars: 12 votes
Frequently Asked Questions
How long do I have access to the course materials?
You can view and review the lecture materials indefinitely, like an on-demand channel.
Can I take my courses with me wherever I go?
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