24. August 2020
Areas: Europe, COVID-19, Russia, Australia, Updates, New regulations and guidances "Issue" 35/20
3. August 2020
Areas: Europe, COVID-19, USA, Australia, Updates, New regulations and guidances "Issue" 32/20
27. July 2020
Areas: Europe, Switzerland, COVID-19, USA, Australia, Updates, New regulations and guidances "Issue" 31/20
24. July 2020
Areas: MDR, MDCG updates, COVID-19, USA, Australia, Malaysia, Taiwan, Updates, New regulations and guidances "Issue" 30/20
9. July 2020
Areas: MDR, COVID-19, USA, Russia, Malaysia, Updates, New regulations and guidances "Issue" 28/20
12. June 2020
Areas: MDR, COVID-19, Canada, Malaysia, UK, Updates, New regulations and guidances "Issue" 24/20
23. May 2020
Areas: MDR, COVID-19, Singapore, USA, Russia, Kazakhstan, Brazil, Canada, Malaysia, China, Updates, New regulations and guidances "Issue" 21/20
8. May 2020
Areas: MDR, FDA, COVID-19, Japan, Taiwan, Malaysia, Updates, New regulations and guidances "Issue" 19/20
24. April 2020
Areas: MDR, COVID-19, IMDRF, Updates, New regulations and guidances "Issue" 17/20
14. April 2020
Areas: MDR, COVID-19, Further EU / MDCG Updates, China, Canada, Updates, New regulations and guidances "Issue" 16/20
26. August 2019
MDR - as of May 26, 2020, a second reporting channel for the disclosure of "non-serious events" or "expected adverse reactions" will be added for all companies.
26. February 2018
For each medical device, clarify exactly which role and thus obligations you have as an economic operator! We will help you with this.