Dataset

A medical device is any instrument or component used to treat, diagnose or prevent a human disease or abnormal physical condition. Page about what medical device problems are and how to report them.

Health Canada information related to adverse reaction reporting of drugs and health products on the Canadian market

Staffing Update Report: April 2022- September 2022

Opioid agonist treatment (OAT) is an effective treatment for opioid use disorder (OUD) as it prevents withdrawal symptoms, reduces cravings, and has been associated with beneficial outcomes such as reductions in illicit drug use and related harms (e.g., overdose, mortality, etc.). To better...

Correctional populations experience high levels of opioid use disorder (OUD) and increased risks for related harms upon the high-risk period of community release and reintegration, including overdose and premature mortality. Opioid agonist therapy (OAT) is an effective treatment for OUD and its...

Child-to-parent violence and aggression (CPVA) is described as a form of family violence characterized by a pattern (as opposed to a single incident) of violent and aggressive behaviours in children and youth towards their parents or primary caregivers. These behaviours may have several...

CSC achieves its public safety goals by effectively managing institutions of different security levels, supervising offenders on various forms of conditional release, and providing programs and services that contribute to ensuring that criminals only end up behind bars once in their life.

This report examines the impact of the lack of access to legal aid in family law cases in Canada. The objective is to identify challenges that people face in accessing justice for family law disputes in the absence of legal aid, and to analyze the impacts of the lack of access to family legal aid...

Staffing Update Report: October 2021 - March 2022

Under IO No. 2, manufacturers and importers must report shortages of specified medical devices (including their components, accessories or parts) of critical medical devices to Health Canada. This new interim order outlines the mandatory reporting requirements.