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 firstname.lastname@example.org and we get back to you. Or come by and visit us in our Booth No. 338.
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
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.