M6 - CE Post Market & Vigilance - Field Safety and Recalls for CE Marked Medical Devices (QP)
PrintPart of Medical Devices QP Training Module 6
£1470.00 exl VAT
About this course
A two day intensive course providing you with the tools necessary to effectively manage the critical aspects of field safety notifications, field safety updates and the specific requirements for withdrawing product from within Europe.
Providing simulations and scenarios the tutors will take you through the decision making processes, plans, risks and considerations to be made in order to manage patient safety, regulatory action and protect company reputation.
Starting with the basic requirements and common methods and then moving into communication strategies, distribution considerations and supply-chain coordination, this course will enable you to manage some of the most complicated and stressful decisions you may experience in the marketplace. Forewarned is forearmed and this course will enable you to make realistic and valuable updates to your field safety and product recall processes.
Who Should Attend
Aimed at all professionals managing a medical device placed on the market and involved in any post market surveillance and vigilance, QMS feedback, clinical follow up and vigilance decision making activities. Authorized representatives and distributors will also find this module highly applicable to their function as critical operators within the supply and post market support of medical devices.
