Open Government Portal

This dataset contains information on Government of Canada tender information published according to the Financial Administration Act. It includes data for all Schedule I, Schedule II and Schedule III departments, agencies, Crown corporations, and other entities (unless specifically exempt) who must comply with the Government of Canada trade agreement obligations. CanadaBuys is the authoritative source of this information. Visit the How procurement works page on the CanadaBuys website to learn more.

All data files in this collection share a common column structure, and the procurement category field (labelled as “procurementCategory-categorieApprovisionnement”) can be used to filter by the following four major …

The primary purpose of the authority codes is to identify expenditure transactions for accountability and reporting in the Public Accounts of Canada according to the specific votes and other authorities in the Estimates, other authorities included in specific statutes; and in addition, to identify the nature of revenue, by tax and non-tax revenue. Other authority codes (non-appropriated authorities) are also established by central agencies to facilitate the identification of various accounting transactions that do not require the use of appropriations. An appropriation is an authority of Parliament to pay money out of the Consolidated Revenue Fund (CRF) and as such, …

This guidance document applies to sponsors intending to make changes to new drugs that have received a NOC pursuant to Section C.08.004 of the Food and Drug Regulations. In the absence of a guidance specific to Quality changes to drugs which were approved through a Drug Identification Application - Biologics (DIN-B drugs), this guidance document applies to those products. This guidance also applies to those submissions for which a NOC has been recommended but issuance of the NOC has been placed on hold.

This guidance document combines and supercedes the policy and guidance documents for Notices of Compliance with Conditions (NOC/c) dated June 12, 2007. The revisions to this document incorporate the provision for the filing of Abbreviated New Drug Submissions (ANDSs) or Supplement to an Abbreviated New Drug Submissions (SANDSs) that reference a Canadian Reference Product (CRP) with NOC/c indications.

The Patented Medicines (Notice of Compliance) Regulations (PM(NOC) Regulations) were introduced originally by Industry Canada under the Patent Act. The PM(NOC) Regulations intersect with drug approval under the Food and Drugs Act and Division 8 of the Food and Drug Regulations.

Notice of Compliance with Conditions - Qualifying Notice.

Notice of Compliance with Conditions - Qualifying Notice.

Notice of Compliance with Conditions - Qualifying Notice

Notice of Compliance with Conditions - Qualifying Notice

Notice of Compliance with Conditions - Qualifying Notice