post-market surveillance Canada

02

Sep

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Medical DevicesCanadian medical device compliance, Class I II III IV medical devices, Health Canada device claims classification, Health Canada medical device licence, Health Canada medical device regulations, ISO 13485 MDSAP Canada, MDEL requirements Canada, MDL application Canada, medical device classification Canada, medical device licensing Canada, post-market surveillance Canada, regulatory consultant medical devices Canada

What You Need to Know About Health Canada’s Medical Device Classifications and Licensing

Whether you are an established medical device manufacturer or entering the Canadian market for the first time, determining the correct classification is the essential first step in licensing your product. An incorrect classification can lead to costly errors, regulatory delays, and extended time to market, ultimately resulting in lost revenue.…

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Contraceptive Device Licensing in Canada: A Quick Overview

08

Jul

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Medical Devicescontraceptive device classification, contraceptive labelling Canada, contraceptive medical devices, contraceptive product compliance, Health Canada medical device licensing, ISO 13485 compliance, IUD licensing Canada, MDEL Canada, MDL Canada, medical device application Canada, medical device regulations Canada, post-market surveillance Canada, regulatory affairs Canada, SNI regulatory support

Contraceptive Device Licensing in Canada: A Quick Overview

The process of bringing contraceptive medical devices to the Canadian market involves navigating a clearly defined but often complex regulatory framework. Products such as intrauterine devices (IUDs), diaphragms, condoms, and contraceptive sponges are considered medical devices and are regulated by Health Canada under the Medical Devices Regulations. This overview outlines…

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