Regulatory Framework for the Review of Human Drugs and Medical Devices

Overview

Delivery method

Online

Duration

–

Audience

Inspectors

Description

Regulatory Framework for the Review of Human Drugs and Medical Devices

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.

Click "Regulatory Framework" to access the course.