22. November 2023
We are celebrating our anniversary. We have been a partner to the healthcare industry for 20 years and support companies with the approval of medical products
20. June 2023
Areas: Europe, Worldwide / Updates, New regulations and guidances 25/23
13. April 2023
Areas: Europe, Worldwide / Updates, New regulations and guidances 15/23
11. April 2023
Post-market surveillance for medical devices as an efficient process for practicability and added value.
4. April 2023
In China, Post Market Surveillance (PMS) is an important component of the regulation for medical devices, ensuring the safety and effectiveness of these products.
31. January 2023
Areas: Europe, Worldwide / Updates, New regulations and guidances 05/23
21. December 2022
Areas: Europe, Worldwide / Updates, New regulations and guidances 51/22
10. November 2022
Areas: Europe, Worldwide / Updates, New regulations and guidances 45/22
1. August 2022
Areas: Europe, Worldwide / Updates, New regulations and guidances 31/22
21. July 2022
Life Cycle management tool support in medical technology. DOORS, RQM or ELM - correctly manage requirements, tests, documentation and traceability.
24. May 2022
Areas: Europe, Worldwide / Updates, New regulations and guidances 20/22
25. April 2022
Areas: Europe, Great Britan, Taiwan, Australia and USA / Updates, New regulations and guidances 15/22