N2 has developed this course on Medical Devices to equip learners with an understanding of the landscape around medical device trials in Canada and to contribute to the safe and effective introduction of innovative medical devices. Content covered includes the regulatory landscape (Canadian versus U.S.), investigator duties, and monitoring and auditing.

This course targets individuals who administer, review, or conduct medical device trials.

Duration: 2:30 hours

Research organizations are increasingly faced with challenges surrounding the management and security of the information they collect and use during the course of conducting research.

N2 has developed this introductory course on Privacy and Security for Personal Information (PI) and Personal Health Information (PHI) in the research environment.

The course is designed to equip learners with an understanding of the privacy legislation around how personal information may be collected, used, shared, accessed and disposed; the fundamentals of records and information management; and leading practices for handling a privacy incident.

This course targets individuals who administer, review, or conduct health research that involves collecting health data, such as during clinical trials.

Duration: 2 hours

This module helps healthcare professionals understand good document practices based on ALCOA-C. At the end of this course, you will be able to:

• Review Source Data, Source Documents and Good Documentation Management
• Review Case Report Forms (CRFs), Electronic Data Capture (EDCs) and Good Data Management
• Review Internal Query Resolution Process

Duration: 20 minutes