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.
Join our webinar to learn about 5 useful tips to plan your internal audits in the most optimized way!
The presentation will be held in Swedish, with material in English.
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.
QAdvis Senior Quality and Regulatory Consultants Camilla Drott and Emma Jansson.
The event is free – register now to participate.
Register at: Eventbrite.
*You will get detailed information for how to attend, in the confirmation e-mail 2-3 days before the event.
Questions: email us or call +46-(0)8-621 01 05.
Communicated cancellations to Academy@qadvis.com.
QAdvis reserves the right to cancel the event due to low attendance, up until 1 week before the webinar start. You can contact us at any time to get a status update. Detailed information and the link for attending will be sent to you 2 days before the webinar starts.
Force majeure QAdvis reserves the right to change teachers or reschedule the course due to force majeure or due to teacher’s illness. No compensation will be paid for any additional costs incurred.
We are longtime trusted providers of MedTech quality and system management, risk management, compliance, training, interim management and regulatory affairs. Offering a thorough knowledge and understanding of the industry, based on 30 years of professional experience, QAdvis have the tools to help take your MedTech innovations to domestic and international markets.