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Students will learn the basic concepts of planning, conducting and report writing for a medical device QMS audit in accordance with ISO 19011:2018. This fast-paced one-day course is a must for auditors at all levels of the organization. You will learn how to apply fundamental auditing strategies to any QMS scheme, as well as how to identify and grade nonconformities and prepare a medical device audit report in accordance with the identified criteria. The course will focus on applying these fundamental principles when auditing medical devices quality management systems.
This ISO 19011:2018 audit training is helpful for all auditors and all management personnel with responsibility for medical device regulatory life cycles, including involvement with the design and implementation of quality management systems or oversight of an internal auditing program.
By the end of this training, you will be able to:
Trained over 1,300 delegates on our CQI and IRCA certified GMP PQS lead auditor training course
Provided expert health sciences training for over 30 years
More people have become ‘Qualified Persons’ in Europe through our training programme than any other training provider
General Registration $600.00
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