Live webinar on Implementing Global Adverse Event Reporting Systems in EU, Canada, and US By Compliance2go October 24, 2012

This webinar is intended to help you get familiar with the medical device adverse event reporting requirements during clinical studies and post-marketing in the EU, Canada and US.
The adverse event reporting is intended to improve the patients’ safety and protection including the users and other stakeholders by preventing the repetitive incidents or by reducing the harmful consequences of the incidents.
Global compliance to the adverse event reporting requirements is imperative to achieve sustainability and to remain sustainable and competitive in global medical device markets during both clinical trials and post-marketing.
It is critical to understand the requirements, establish and maintain a medical device adverse event reporting system. To do so, this webinar will present a practical and actionable strategy to streamline the process by employing a “CAC-SI” method.”

Official Website: https://compliance2go.com/index.php?option=com_training&speakerkey=27&productKey=183