An NSF International Company M5 - Global Quality System Requirements - Introduction to ISO 13485 (QP)
PrintPart of Medical Devices QP Training Module 5
£735.00 exl VAT
About this course
Whether you are working toward the registration of your first CE marked product or you are wanting to diversify into the medical device supply chain, ISO 13485 is the standard required for all regulatory aspects associated with your processes. This course takes you through how to plan and execute an implementation project, enabling you to walk away understanding exactly what needs to be done and how to successfully implement ISO 13485 within your organization.
Who Should Attend
Aimed towards professionals responsible for the development of quality management systems for medical devices. The course will certainly benefit new start-up companies as they will be able to implement a quality management system against the requirements of ISO 13485 and CFR21 part 820. Qualified Persons in pharmaceutical manufacturers will find this course highly beneficial if they are working with a new division providing a medical device or if they need to work with a supplier based upon implementation of an effective QMS.
