Quality Management Systems for Distributors (QMS) Under EU MDR
Distributors of medical devices in the European Union play a vital role in ensuring product safety, traceability, and regulatory compliance. […]
MDR Quality Management
MDR Responsibilities
Legal Responsibilities of a Medical Device Distributor | EU MDR Compliance
Distributors serve as a critical link in the medical device supply chain, connecting manufacturers with end users such as hospitals,
MDR Overview
What is the EU Medical Device Regulation (EU MDR)?
The EU Medical Device Regulation (EU MDR 2017/745) is one of the most significant regulatory changes in the European medical
MDR Overview
The EU MDR Distributor Responsibilities
The European Union’s Medical Device Regulation (EU MDR 2017/745) establishes strict requirements for medical device distributors operating within the EU
MDR Overview
MDR for Distributors: What You Need to Know
Why MDR Compliance Matters for Distributors If you distribute medical devices in the EU, the Medical Device Regulation (MDR 2017/745)