Health Canada Product Registration Database

Health canada medical device and quality management system requirements when applying for an mdl, you will also need to prove that you have a certified iso 13485 quality management system under the medical device single audit program (mdsap), which meets the specific requirements of the canadian medical devices regulations (cmdr). The database is openly accessible by anyone and the public can search for devices by using the device name, product owner, identification number, or. Class b, c, and d devices require registration.

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Database of pesticide product information from health canada's pest management regulatory agency.

Health canada product registration database. This data extract contains information on nhp products. Registration requirements vary per submission type, class of fertilizer or supplement and risk profile of the product. Natural health products regulations [219 kb] | pdf full document:

You can search for different drugs with. The bureau maintains a database of all licensed class ii, iii, and iv medical devices offered for sale in canada. Canada's crops and forests are protected by the cfia's ongoing efforts related to the regulation of plant supplements and fertilizers.

Report a problem on this page. This database houses all incident reports for canadian marketed pesticides that have been submitted to health canada. Step 6 health canada reviews mdl application (class ii, iii and iv) and premarket review document (class iii and iv only).

Availability of the drug in canada ; Releasable establishment registration and listing information under the freedom of information act is available by searching the establishment registration and listing database. Health canada will invoice fees over $5000.

Departments of environmental health in the health bureaus (hebrew) freedom of information in environmental health; Product monograph (pm) for human drugs ; Drug product database online query from health canada due to the fact that the information originated with an organization that is not subject to the official languages act, the document may only appear in the language in which it was written.

This upgraded version allows you to search, sort and filter information on application, product, active ingredient, and incident reports. Alternatively, you may use form fda 3741 for establishment registration and product listing. An electronic health record (ehr) is a prime example of such an application.