An NSF International Company M5 - Global Quality System Requirements - ISO 13485 Advanced - Effective CAPA Investigations (QP)
PrintPart of Medical Devices QP Training Module 5
£735.00 exl VAT
About this course
In order to undertake corrective and preventive action effectively there is a need to understand exactly what constitutes good practice. This course is aimed towards helping you to identify CAPA opportunities and takes you through how to effectively investigate using the information and tools available within your organization. As a medical device manufacturer it is critical that CAPA is effective and it is a common expectation by regulatory agencies that this is one of the most robust processes within your organization. Learn how to manage CAPA effectively, from identifying and managing sources of CAPA to the effective implementation of corrective actions.
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.
