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
Post-market surveillance and vigilance (PMSV)
June 19 2024
Navigate the risk management maze: Benefit-risk analysis made easy
March 21 2023
What is going on in Brussels
February 14 2023
In Vitro Diagnostic Regulation 2017/746 (IVDR)
January 19 2023
5 Ways to optimize your internal audits
June 1 2022
UKRP Presentation Webinar
May 2 2022
Usability engineering according to IEC 62366-1
December 15 2021
QAdvis MDR and IVDR latest update
March 10 2021
UK Responsible Person
November 13 2020
Lost in the jungle of standards?
September 3 2020
MDR – 9 months to go
August 27 2020 – Status and some reflections
Navigate the Risk Management Maze Webinar
June 17 2020 – 5 tips for successful MDR transition
Technical Documentation Webinar
June 5 2020 – Short introduction to how create effectively technical documentation needed for medical devices. In Swedish.
Health Apps Webinar
June 2 2020 – Short introduction to IEC 82304-1 and IEC 82304-2. In Swedish.
IVDR Webinar
April 16 2020 – Fundamentals you need to know. Latest updates, How to prepare
A short introduction – 191014
Intro to the MDR & IVDR SW Guidance
Breakfast seminar – MDR
24 and 26 September 2019
MDR and medical device software
January 2020
Breakfast seminar
Whats new in the ISO 14971:2019 standard?
Breakfast seminar
Medical device SW – challenges in the EU by Robert Ginsberg
Regulatory summit
Rule 11 in MDR –practical considerations
by Robert Ginsberg
Breakfast seminar – IVDR
Fundamentals you need to know,
Latest updates, How to prepare
Breakfast seminar
What can we expect in the new revision of ISO 14971
MDR – IVDR seminar
Intro to MDR and IVDR
MDR – IVDR seminar
Clinical Evaluation & Clinical Performance Evaluation
Breakfast seminar
Software Tool Validation
Breakfast seminar
Ready – Set – MDR
Breakfast seminar
Lost in the standards jungle?
Breakfast seminar
MDR and its potential impact on Technical Files
QAdvis-agile-development w WM
Agile software development for Medical Devices
QAdvis sw-rm-webinar w WM
The role of Risk Management in EN 62304
Breakfast seminar
QAdvis-mdd w WM (Swedish)
Introduction to ISO/IEC 80001-1
Application of Risk management for IT-networks incorporating Medical devices
Webinar
The benefits of a Quality Management System
Breakfast seminar
ISO 13485:2016 – What’s new – and what does it mean?
Breakfast seminar
UDI – Final rule
Breakfast seminar
Common mistakes in technical files
Breakfast seminar
IEC 82304-1 fills the gap
Seminar RMD
How to make IEC 62304 and IEC 82304-1 work
Video
Video 5 Ways to optimize your internal audits
June 1 2022
Video UKRP Presentation Webinar
May 2 2022
Video Usability engineering according to IEC 62366-1
December 15 2021
Video UK Responsible Person
November 13 2020
Video Lost in the jungle of standards?
September 3 2020
Video Navigate the Risk Management Maze
June 17 2020 – Five tips for successful MDR transition
Video Technical Documentation
June 5 2020 – Short introduction to how create effectively technical documentation needed for medical devices. In Swedish.
Video Health Apps
June 2 2020 – Short introduction to IEC 82304-1 and IEC 82304-2. In Swedish.
Video IVDR Webinar
April 16 2020 – Fundamentals you need to know. Latest updates, How to prepare
Video Breakfast seminar – IVDR
Fundamentals you need to know. Latest updates, How to prepare
Video Breakfast seminar
Ready Set MDR (Swedish)
Video Breakfast seminar
MDR and its potential impact on Technical Files (Swedish)
Video Breakfast seminar
Technical Files 2016-11-24 (Swedish)
QAdvis is a solution-oriented trusted service provider for the medical device and in vitro diagnostic device sector. To enable and maintain global market access, we can with high level of knowhow and expertise within quality management and regulatory affairs support your company to be in compliance with applicable regulations and requirements. QAdvis was founded in 2013 and is based in Sweden. We are certified according to ISO 13485:2016.
