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
Risk Management | Software and Cybersecurity | Marketing approval for medical devices, MD and IVD
Clinical evaluation and Performance evaluation | Biocompatibility assessment | Quality Management System for medical device manufacturers
PMS – Post Market Surveillance | Due Diligence | Usability | Acccess the European Union (EU) | Acccess the UK
