1. April 2022qtec Spotlight – Focused expert knowledge on medical technologyQtec Spotlight is our focus on current topics from the medical device life cycle. Every quarter, our experts shed light on a specific area.
16. March 2022Regulatory Affairs Update 11/22Areas: Europe, Great Britan, Taiwan, Australia and USA / Updates, New regulations and guidances 11/22
14. February 2022Clinical Investigations and PMCF Studies under the MDR: Correct Classification and ApplicationBrauchen Klinische Prüfungen und PMCF-Studien eine Prüfung durch die Ethik-Kommission? Erfahren Sie, wie PMCF-Studien einzuordnen sind.
11. February 2022Regulatory Affairs Update 06/22Areas: Europe, Great Britan, Taiwan, Australia and USA / Updates, New regulations and guidances 06/22
28. October 2021Impact of the MDR on Quality Assurance Agreements (QAA)We will show you why a quality assurance agreement is an important and central document of the MDR, and should make sure it is always up to date.
20. October 2021Regulatory Affairs Update 42/21Areas: Europe, USA, Australia / Updates, New regulations and guidances 42/21
6. October 2021Regulatory Affairs Update 40/21Areas: USA, Australia, Singapore, India / Updates, New regulations and guidances 40/21
7. September 2021Regulatory Affairs Update 35/21Areas: Europe, USA, Australia, India, Taiwan / Updates, New regulations and guidances 35/21
11. August 2021Regulatory Affairs Update 32/21Areas: Europe, Worldwide, Myanmar, Indian, Australia, Singapore, Canada, China / Updates, New regulations and guidances 32/21
16. June 2021Regulatory Affairs Update 24/21Areas: Europe, Australia, USA / Updates, New regulations and guidances 24/21
2. June 2021Regulatory Affairs Update 22/21Areas: Europe, Taiwan, Australia, Singapore / Updates, New regulations and guidances 22/21
11. May 2021Regulatory Affairs Update 19/21Areas: Europe, India, Singapore, Taiwan / Updates, New regulations and guidances 19/21