We’re on a mission to equip everyone who works with, supports, or cares about survivors of IPV with the knowledge and tools needed to recognize BI and respond appropriately in every case.

There is currently a lack of centralized resources and community connections for professionals and researchers working with IPVBI survivors. The existing resources are fragmented, causing inefficiencies and barriers in accessing critical information and support; and hindering the ability of service providers and researchers to effectively support survivors and advance the field.

Addressing these issues is crucial. The field of IPVBI research is in its infancy, with only a small number of dedicated professionals. By creating a centralized hub, we can prevent the chaos of scattered resources, enhance collaboration, and provide a blueprint for community support.

The Canadian Centre for IPV-BI was created to fill a critical gap  in IPV-BI knowledge and practice. 

What We Do

A Pan-Canadian Effort

The Canadian Centre for IPV-BI is part of a national strategy to improve public and service provider knowledge and awareness of IPV-BI. The strategy aims to equip multi-sector service providers with the training, tools, and resources they need to recognize and respond to IPV-BI.

Our ongoing goals include:

  1. Deliver online educational and training courses to ensure universal access to key information for healthcare and social support providers working with women who have experienced IPV-BI.
  2. Equip  healthcare and support providers with resources such as standardized tools, recommendations on how to use them, and next steps for care options.
  3. Work together  with key stakeholders to strengthen community capacity to recognize and respond on a local level while continuing to contribute to a national strategy to address IPV-BI.