Short Course Registration: 7:00-8:00AM
This session will give an overview of how the regulatory process unfolds in HPFB and how the Branch develops supporting policy, guidance documents, and processes. The session will describe the regulatory and policy processes, how comments are sought from stakeholders and incorporated in policy and regulatory decision-making, some lessons learned, and best practices in these areas, including case examples from both Health Canada and Industry.
*Short Courses are not included in the meeting registration and require a separate fee.
Return to DIA Annual Canadian Meeting
At the conclusion of this short course, participants should be able to:
- Describe the Canadian context of key policy and regulatory issues in HPFB
- Review processes and practices that take place in HPFB on the development of policy, guidances, and regulations
- Explain the policy and regulatory development process and the role of stakeholders