Access UK
Partner with QAdvis for your UK Responsible Person
QAdvis is an expert in quality and regulatory compliance within the medical device industry. One of our key competences is to support non-UK manufactures of medical devices to comply with UK directives and regulations through our UK Responsible Person services. Our UK-based company QAdvis UK Ltd is also one of the founding members of the UK Responsible Person Association (UKRPA).
The Process – From Contact to Maintenance
An insight into UKRP
with Per Sundström
More related information:
Contact us for our UKRP services
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.
