Master medical devices registration in Canada

Manage all regulatory activities of medical devices in the market of Canada

3.95 (23 reviews)
Udemy
platform
English
language
Industry
category
Master medical devices registration in Canada
78
students
2.5 hours
content
Feb 2022
last update
$44.99
regular price

What you will learn

Master Medical devices registration in Canada

Manage all regulatory activities of medical devices in Canada

Place your medical devices in the market of Canada

Master the medical devices market of Canada

Why take this course?

Master medical devices registration in the most important and biggest market ever in the world, the market of Canada, 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 more than half of the revenue for such a company on one hand while on the 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 Canada.

Dear pharma industry future professionals, let us start our interesting journey toward medical device registration in the states, we will travel together to the states, meet the health authority there "HC", and explore its requirements for registration, renewal, and variations, let us get our "HC" approval and place our products there.

In this course, we will cover all topics related to medical devices in Canada, starting from the requirements, interim regulations, classification, verification, special conditions, and weavings

And finally, congratulations to you for mastering medical device registration in the Canadian market, and see you soon in the pharma industry my dear colleagues.



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Reviews

Hiralkumar
November 8, 2022
Great explain all topics. Kindly make more video on" Health Canada regulatory submission for pharmaceutical products" & on "ICH guildlines ".
Tata
July 15, 2022
It is really interesting that from time to time, the lecturer points out where the MDR system of Canada differs or relates with MDR in other areas like the EU, UK etc. The course is so enriching.
Diane
February 10, 2022
Dr. Zahra Hassan did an amazing job of thoroughly explaining the Regulatory system in Canada. She took the time to make quality graphics and provided useful links to use for future reference. Equally enjoyed the comparisons between the different regions of the world which helped link the regulatory process even further. Thanks for taking the time to do such a great job!!

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4380142
udemy ID
11/3/2021
course created date
11/14/2021
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