21 November, 2023
New EU GMP Annex 1 is applicable as of August 25, 2023!
At GXP CONSULTING Switzerland, we are committed to supporting our clients through this transition. We offer specialized training sessions on the new Annex 1 and provide gap assessment services to ensure your operations comply with it. If you are interested in learning more or engaging with our experts, please don't hesitate to contact us.
20 July, 2022
Breaking News: our new alliance with Group IPS
We are proud to announce our new alliance with Group IPS, a key partner for project management, engineering (EPCM), and a vast range of specialized services. Thanks to this partnership we are covering all stages of our clients' project life cycle.
26 April, 2022
GXP CONSULTING Switzerland 8th anniversary!
We are happy to have blown our 8th candle and are very proud of our major achievements realized thanks to the commitment of all our talented team and the trust of our numerous customers! GXP CONSULTING Switzerland has become a major player in Switzerland with a very good reputation and brand image. What a journey, and this is just the beginning of an even more incredible adventure that awaits us!
28 July, 2021
Our article about the European Medical Device Regulation (MDR)
The European Medical Device Regulation (MDR) is a new set of regulations that governs the production and distribution of medical devices in Europe. We have published this article to take a step back and remember where it came from and how crucial a transition from MDD to MDR is for an optimised, safe and performing medtech industry. If you have questions or your need support, please let us know, we are at your disposal!
