Health Canada is the apex regulatory body for ensuring safety, effectiveness, and quality of medical devices entering the Canadian market. Complying with Health Canada medical device regulations is a must to launch your product in Canada. Moreover, you have to secure...
To simplify and expedite the import process for already-approved medical devices and IVDs, CDSCO has implemented a new provision. A circular dated 15.9.25, states that w.e.f 11.9.25 a separate provision for “Subsequent Importers” of already-approved...
Health Canada medical device labelling guidelines are designed to ensure the device’s use is clearly understood by users. These guidelines help patients and practitioners use the device as intended. Hence, the medical device labelling guidelines have a role in device...
Health Canada issues two types of licenses, medical device establishment licence (MDEL) and medical device licence (MDL). Medical devices are categorised into Class I, II, III, and IV, based on risk level. It is important to determine the class to which your medical...
To secure CE mark, the manufacturer is expected to ensure all EU-wide requirements for the medical device have been complied. If the device complies with strict safety, health, and environmental protection benchmarks, it may be granted the CE mark certification....