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Join our webinar to learn about 5 useful tips to plan your internal audits in the most optimized way!
The ISO 13485 requirement to conduct internal audits may be a challenge for organisations in the medical device business. To fulfil the standard requirements and at the same time use the internal audits as valuable feedback for the organisation – and not use more resources than necessary, is a puzzle for quality managers and their staff to solve.
The presentation will be held in Swedish, with material in English.
Location
The webinar will be administrated as a Zoom webinar.
You will get detailed information for how to attend, in the confirmation email 2 days before the event.
Speakers
Senior Quality and Regulatory Consultants
Camilla Drott and Emma Jansson.
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