QAdvis participated in the event Kista All Stars in June, to connect and celebrate together with other amazing companies that all had achievements and awards to be proud of.
A great possibility for inspiration and to meet others and network with our neighbors in Kista Science City, as well as getting inspired by fantastic people outside of the MedTech industry.
Read more here: Framtiden finns bland stjärnor i Kista – Kista Science City
QAdvis want to congratulate their customer, Combinostics Oy, for achieving their MDR certificate with help from our highly skilled consultants.
The transfer to MDR and/or IVDR is crucial for medical device manufacturers, to maintain market access in Europe.
We are proud that we can be part of that journey for several customers, guiding as well as providing hands-on work during both the implementation and certification process.
“QAdvis has been invaluable to Combinostics Oy in achieving this significant milestone. We are proud to be certified under MDR and look forward to enhancing the care of patients with neurodegenerative diseases through the use of our digital AI solutions”
Lennart Thurfjell, PhD, COO Combinostics Oy
The management team at QAdvis is delighted to announce that Annelie Hagström has been appointed as a new site manager in Lund starting from June 2022. Annelie is one of our Senior Quality and Regulatory consultants and has a broad and extensive experience within the medical device area and business development. She will continue to support our clients as a consultant in parallel with the role as site manager.
We are convinced that this will further strengthen our internal structure for the future and be of great benefit to our clients.
Meet our new CEO Emma Axelsson and listen to three of our consultants Cecilia Emanuelsson, Nils Lidström and Per Sundström at the upcoming Regulatory Summit hosted by Swedish Medtech on March 31.
For the 5th year in a row, Swedish Medtech is holding a regulatory conference and interest in the subject is growing every year.
QAdvis both exhibits and has several speakers at this years Swedish Medtech Regulatory Summit. Come and meet us in our stand and take the opportunity to listen to our business offer, our visions for the future and ask your questions directly. In addition, you also have the opportunity to listen to some of our consultants presenting during the day.
There will also be presentations by the Swedish competent authority for medical devices (Läkemedelsverket), and MedTech Europe will give a picture of the complex reality and challenges ahead.
Take the opportunity and visit us in our exhibitor stand at Regulatory Summit, this year at Hilton, Slussen in Stockholm, 31 March.
Read more here – Regulatory Summit Swedish Medtech
QAdvis is a solution-oriented trusted service provider for the medical device and in vitro diagnostic device sector. To enable and maintain global market access, we can with high level of knowhow and expertise within quality management and regulatory affairs support your company to be in compliance with applicable regulations and requirements. QAdvis was founded in 2013 and is based in Sweden. We are certified according to ISO 13485:2016.
