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This is the requirement from HC site:
Did anyone have any first hand experience with discontinuing product which was licensed for sale in Canada. I was wondering specifically if you would obsolete the product technical documentation right away or would you wait the lifetime of the device, or.. ? How about other countries, would you have to inform them right away of your product being terminated for sale in Canada or could you wait the next registration cycle to inform them.
Many thanks in advance.
The manufacturer must inform the regulator within 30 days after discontinuing sale of their medical device in Canada, in order to cancel the licence.
Did anyone have any first hand experience with discontinuing product which was licensed for sale in Canada. I was wondering specifically if you would obsolete the product technical documentation right away or would you wait the lifetime of the device, or.. ? How about other countries, would you have to inform them right away of your product being terminated for sale in Canada or could you wait the next registration cycle to inform them.
Many thanks in advance.
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