Learning catalogue - Health Canada & the Public Health Agency of Canada

This workshop will cover simple actions you can take to make your PowerPoint presentations accessible to people with different accommodation needs. Accessibility best practices are essential to ensure that everyone feels included in the workplace.

This course is designed to assist scientific reviewers with the preparation of an in vitro diagnostic medical device licence (MDL) application evaluation report under the Medical Devices Regulations. Each module will cover what you should look for when you are reviewing a specific topic within an application and tell you what should be included in your report.

This course is designed to assist scientific reviewers with the preparation of a medical device licence (MDL) application evaluation report under the Medical Devices Regulations.

You will learn the respective roles and responsibilities involved in preventing and responding to Work Place Harassment and Violence. You will also evaluate work place scenarios, and determine when and how to initiate a Notice of Occurrence.

The Privacy Basics and Privacy Impact Assessments course has been developed to provide you, as a federal government employee, with an overview of the legislative and policy framework that governs the protection of personal information in federal government institutions.

This course is intended for anyone who needs to understand and address quality issues. It will provide basic information on quality concepts and should help you identify quality issues in the workplace. After completing this course, you will be better prepared to participate in quality initiatives. This course focuses on knowledge and understanding, rather than skills and techniques.

This e-learning course will provide an understanding of the Quarantine Act and how it applies to the role of a Quarantine Officer. The Quarantine Act will be reviewed with examples, comments and scenarios of how it is implemented in the field.

The Quarantine Scenarios online training course will provide learners with the opportunity to apply the knowledge they have gained from the prerequisite courses [Roles and Responsibilities of Quarantine Officers, Key Partners and Players; Quarantine Act; and Public Health Emergency of International Concern (PHEIC)]. Using scenarios, learners will solve complex problems similar to those encountered in real life within the Quarantine Program, taking into account the theory, policies and procedures required to understand the scenarios presented, and the interventions expected. This training will assist in preparing learners for potential public health situations by anticipating appropriate independent and team responses.

This course, as part of a Radiation Safety Program, is designed to provide information and guidance pertaining to radiation safety during receipt, storage, handling, and disposal of radioactive materials.

Through explanations, suggestions, examples and exercises, this course is designed to give new reviewers within the Health Products and Food Branch (HPFB) an overview of the regulatory framework for the review of human drugs and medical devices. Throughout this course, users will learn about the basics of the regulatory framework. Acts and Regulations will not be discussed in detail in this course. For more information on Acts and Regulations, see the classroom course entitled Administrative Law and the Issuance of Market Authorizations for Drugs.

Regulatory Framework for the Review of Human Medical Devices and Pharmaceuticals Through explanations, suggestions, examples and exercises, this course is designed to give new reviewers within the Health Products and Food Branch (HPFB) an overview of the regulatory framework for the review of human drugs and medical devices. Throughout this course, users will learn about the basics of the regulatory framework. Acts and Regulations will not be discussed in detail in this course. For more information on Acts and Regulations, see the classroom course entitled Administrative Law and the Issuance of Market Authorizations for Drugs.