AMDR filed comments to the European Commission’s Inception Impact Assessment on Waste Shipment Regulations
AMDR appreciates the Commission’s communication on a European Green Deal and efforts to mobilize industry for a clean and circular economy. Solutions like medical device remanufacturing help promote a more resilient, cost-effective, and environmentally sustainable
Health Care Business News: Supply chain lessons emerging from the coronavirus pandemic
How hospitals can reduce costs and better control their supply chain will be particularly relevant as administrators and clinicians prepare for the reopening of service lines that have been shut down during the coronavirus crisis.
Compliance Navigator BSI: Reuse of single-use medical devices in the European Union
Article 17 of the European Medical Devices Regulation 2017/745 (MDR) covers reprocessing of single-use medical devices. It indicates that reprocessing of single-use devices is only permitted if specifically allowed by national law in a Member State.
AMDR Files Amicus with U.S. Supreme Court in Computer ‘Hacking” Case
A case before the Supreme Court may imperil consumers' ability to access and repair computers they own – including medical devices. The implications of the ruling could have major implications for patients, the healthcare supply
AMDR Issues Amicus Brief on Consumer Protections
Hospitals’ Ability to Control and Maximize the Value of Medical Devices at Heart of Amicus Brief to the Supreme Court Association of Medical Device Reprocessors submits amicus brief to U.S. Supreme Court ahead of hearing
Catheter Ablation Technology and the Circular Economy
Catheter ablation is one of the fastest growing service lines in U.S. healthcare. More and more patients are diagnosed with atrial fibrillation (AFib) and similar conditions, and electrophysiology (EP) labs are treating them as fast