Drug & health product inspections drugs made in canada or abroad must meet high safety and quality standards before they can be sold to canadians. There are several search options:
This data extract contains information on nhp products.
Health canada product registration database. This upgraded version allows you to search, sort and filter information on application, product, active ingredient, and incident reports. Fdb is the #1 provider of integrated drug and medical device databases that support healthcare professionals to make precise decisions. The licensed natural health products database contains information about natural health products that have been issued a product licence by health canada.
An oltp database is one that a single computer application runs on. The database is openly accessible by anyone and the public can search for devices by using the device name, product owner, identification number, or. This database houses all incident reports for canadian marketed pesticides that have been submitted to health canada.
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. Availability of the drug in canada ;
The dpd is updated nightly and includes: Natural health products regulations [219 kb] | pdf full document: You can search for different drugs with.
You can be more than 1 classification with health canada. An electronic health record (ehr) is a prime example of such an application. Releasable establishment registration and listing information under the freedom of information act is available by searching the establishment registration and listing database.
Report a problem on this page. 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 8th edition of the vienna classification system is used to index canadian trademarks available on this database.
Registration requirements vary per submission type, class of fertilizer or supplement and risk profile of the product. Alternatively, you may use form fda 3741 for establishment registration and product listing. Product regulated but exempt from registration.
Welcome to the new and improved version of the pesticide product information database. Search the drug product database (dpd) to find drugs authorized for sale by health canada. It is designed to be completed online and saved at any time to your workstation.
Generic drug manufacturers must update their pm to ensure it aligns with the canadian. Class i medical devices do not require a medical device licence and are monitored by the health products and food branch inspectorate (compliance and enforcement) through establishment licensing. The singapore medical device register (smdr) is a database that contains a list of all medical devices that are currently being used on patients.
The bureau maintains a database of all licensed class ii, iii, and iv medical devices offered for sale in canada. Class b, c, and d devices require registration. Through an active internet connection, the web pla form searches and populates data from the natural health products ingredients database (nhpid).
Evidence demonstrating this must be submitted to health canada by means of a product license application (one for each product). The government of canada (gc) licenses and regularly inspects companies that make, package, test, import, distribute and wholesale drugs. Departments of environmental health in the health bureaus (hebrew) freedom of information in environmental health;
Health canada will invoice fees over $5000. Name of manufacturer and owner of the registration in israel, type of packaging and price. Step 7 for class i devices, approved applications will be posted on the health canada website and your mdel certificate will be emailed to you.
The vienna codes describing figurative elements of the trademark can be added to further refine your search. Regulations and registration of additives used in the production of cannabis. Canada's crops and forests are protected by the cfia's ongoing efforts related to the regulation of plant supplements and fertilizers.
Initial search page for the drug and health product register Step 6 health canada reviews mdl application (class ii, iii and iv) and premarket review document (class iii and iv only). Database of pesticide product information from health canada's pest management regulatory agency.
Database of pesticide product information from health canada's pest management regulatory agency.