Free Seminar – Incident Reporting/PMS – 19 June – Kista
Let’s talk about incident reporting, one of the important Post Market Surveillance activities for ...
Author Aurevia:
Leveraging clinical quality registries for innovative clinical trials
Innovation in clinical trials is vital for the future of medical research and development, and ...
Free Seminar – Incident Reporting/PMS – 13 June – Lund
Let’s talk about incident reporting, one of the important Post Market Surveillance activities for ...
Will AI replace your doctor?
AI enabled medical devices are increasingly making their way into every sector of the medical ...
Importers and Distributors: Pivotal roles in MDR and IVDR Compliance
There is a common misconception that only manufacturers need to comply with the Medical Device ...
We strengthen our team
A warm welcome to Marie Mathiasson, our new team-member in Kista QAdvis is happy to welcome Marie ...
Does the requirement for an independent person at design reviews no longer apply?
The FDA’s recent implementation of the Quality Management System Regulation (QMSR) introduces ...
Can supply problems potentially result in shortages of medical devices in hospitals?
In recent years, significant disruptions in global supply chains have had a huge impact on ...
Join us at the Swedish Medtech Regulatory Summit on 14 March 2024
QAdvis will attend the yearly Regulatory Summit hosted by Swedish Medtech. This year Robert ...