QAdvis is now officially part of Aurevia. This change of name follows our company’s integration into Aurevia. The Aurevia brand was born in January, when Labquality, Artimed, Clinical Consulting, Kasve, and Prisma CRO merged under the same name. With QAdvis now proudly joining the team, we are further strengthening our expertise and services and together offering greater value to our joint customers. Scandinavian CRO is also joining Aurevia.
We welcome a new team member – Cristina Barkman
Cristina has a solid academic and industrial background, entirely focused around medical devices. She supports both larger corporations and start-ups with quality and regulatory, in particular complex product development and risk management aspects. Cristina is located in our Lund office. Read more about Cristina here.
We are delighted to welcome Ekaterina Riabova to our team
Ekaterina is located at our Lund office. She brings many years of medical device experience to our team and clients, and she has a strong academic background with a Ph.D. in Bioinorganic Chemistry. Read more about Ekaterina here.
QAdvis enters partnership with Everdon Security
QAdvis has signed letter of cooperation with the Swedish cyber security company Everdon Security. The intention is to offer better regulatory services, information security and risk management to enterprises in the cross roads of medtech, medical software and security. QAdvis is a long-term expert in quality and regulatory requirements and implementation, together with Everdon we […]
Meet QAdvis at RAPS in Washington
QAdvis is an exhibiter at the “The annual Regulatory Convergence in Washington” September 9th – 12th. If you are interested in scheduling meeting please send a mail to info@qadvis.com and we get back to you. Or come by and visit us in our Booth No. 338.
Robert Ginsberg speaker at RMD Europe 2017
Robert Ginsberg is a speaker at the 2nd European Symposium on The New Agreed Draft Regulations on Medical Devices. The event is in Berlin October 16th – 17th. Robert’s speech is about medical software regulation and compliance and is on the 17th at 2 pm. Read more at RMD Europe 2017