Previous presentations, seminars
and webinars

Here you will find our previous presentations, seminars and webinars. If you have any questions,
feel free to contact us at academy@qadvis.com

Presentations

Navigate the risk management maze: Benefit-risk analysis made easy
March 21 2023

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What is going on in Brussels
February 14 2023

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In Vitro Diagnostic Regulation 2017/746 (IVDR)
January 19 2023

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5 Ways to optimize your internal audits
June 1 2022

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UKRP Presentation Webinar
May 2 2022

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Usability engineering according to IEC 62366-1
December 15 2021

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QAdvis MDR and IVDR latest update
March 10 2021

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UK Responsible Person
November 13 2020

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Lost in the jungle of standards?
September 3 2020

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MDR – 9 months to go
August 27 2020 – Status and some reflections

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Navigate the Risk Management Maze Webinar
June 17 2020 – 5 tips for successful MDR transition

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Technical Documentation Webinar
June 5 2020 – Short introduction to how create effectively technical documentation needed for medical devices. In Swedish.

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Health Apps Webinar
June 2 2020 – Short introduction to IEC 82304-1 and IEC 82304-2. In Swedish.

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IVDR Webinar
April 16 2020 – Fundamentals you need to know. Latest updates, How to prepare

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A short introduction – 191014
Intro to the MDR & IVDR SW Guidance

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Breakfast seminar – MDR
24 and 26 September 2019

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MDR and medical device software
January 2020

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Breakfast seminar
Whats new in the ISO 14971:2019 standard?

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Breakfast seminar
Medical device SW – challenges in the EU by Robert Ginsberg

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Regulatory summit
Rule 11 in MDR –practical considerations
by Robert Ginsberg

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Breakfast seminar – IVDR
Fundamentals you need to know,
Latest updates, How to prepare

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Breakfast seminar
What can we expect in the new revision of ISO 14971

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MDR – IVDR seminar
Intro to MDR and IVDR

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MDR – IVDR seminar
Clinical Evaluation & Clinical Performance Evaluation

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Breakfast seminar
Software Tool Validation

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Breakfast seminar
Ready – Set – MDR

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Breakfast seminar
Lost in the standards jungle?

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Breakfast seminar
MDR and its potential impact on Technical Files

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QAdvis-agile-development w WM
Agile software development for Medical Devices

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QAdvis sw-rm-webinar w WM
The role of Risk Management in EN 62304

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Breakfast seminar
QAdvis-mdd w WM (Swedish)

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Introduction to ISO/IEC 80001-1
Application of Risk management for IT-networks incorporating Medical devices

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Webinar
The benefits of a Quality Management System

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Breakfast seminar
ISO 13485:2016  – What’s new – and what does it mean?

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Breakfast seminar
UDI – Final rule

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Breakfast seminar
Common mistakes in technical files

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Breakfast seminar
IEC 82304-1 fills the gap

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Seminar RMD
How to make IEC 62304 and IEC 82304-1 work

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Video

Video 5 Ways to optimize your internal audits
June 1 2022

See video (YouTube)

Video UKRP Presentation Webinar
May 2 2022

See video (YouTube)

Video Usability engineering according to IEC 62366-1
December 15 2021

See video (YouTube)

Video UK Responsible Person
November 13 2020

See video (YouTube)

Video Lost in the jungle of standards?
September 3 2020

See video (YouTube)

Video Navigate the Risk Management Maze
June 17 2020 – Five tips for successful MDR transition

See video (YouTube)

Video Technical Documentation
June 5 2020 – Short introduction to how create effectively technical documentation needed for medical devices. In Swedish.

See video (YouTube)

Video Health Apps
June 2 2020 – Short introduction to IEC 82304-1 and IEC 82304-2. In Swedish.

See video (YouTube)

Video IVDR Webinar
April 16 2020 – Fundamentals you need to know. Latest updates, How to prepare

See video (YouTube)

Video Breakfast seminar – IVDR
Fundamentals you need to know. Latest updates, How to prepare

See video (YouTube)

Video Breakfast seminar
Ready Set MDR (Swedish)

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Video Breakfast seminar
MDR and its potential impact on Technical Files (Swedish)

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Video Breakfast seminar
Technical Files 2016-11-24 (Swedish)

See video (YouTube)