Attend this online training to learn how to plan perform and report internal MDSAP audits. In this training you’ll get to know best practice and tools you can utilize when preparing to undergo or perform MDSAP audits. It covers the requirements MDSAP place on a Quality Management System and also the relationship between MDSAP, ISO13485:2016 and national regulatory requirements.
After this 4-hour course you will be better equipped to tackle the questions above. We’ll walk you through the key MDSAP requirements on the Medical Device quality management systems and provide you with tools to perform an efficient MDSAP gap analysis of your quality system. The relationship between ISO13485:2016 and MDSAP will be discussed and requirements not covered by the standard pointed out.
The requirements posed on the legal manufacturer will be explained, and also how to define and document relationships to other parties, such as the NB, subcontractors, suppliers and between an OBL manufacturer and the OEM.
Finally, we will cover how the participating countries make use of MDSAP audit outcome in their evaluation of devices and manufacturers.
In this course you will learn how to:
Completion of this course will give you the knowledge needed to 1) assess your current quality management system for MDSAP compliance and 2) plan and perform an internal MDSAP-audit
The course is suitable for persons involved in, or responsible for the operation or audit of a Quality Management System for medical devices who need to perform internal audits against MDSAP, or prepare the organization for upcoming MDSAP audits.
This course is available as an In-House Training course. Let us know if you wish to customize a course or if you are a large group with the same requirements.
Leading specialist with long experience of training are guiding you through regulations, guidelines, interpretations, requirements and applications.
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