The regulations will entry into force 20 days after publication in the EU Official Journal. Publication is expected to occur in May.
Welcome Emma! Emma is located at our Stockholm office. Read more about Emma here.
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.