Regulated Reprocessed / Remanufactured Devices Expand to EU
We have some important news coming out of the EU! Two months from now, on May 26 2020, the EU MDR will officially go into effect, thus establishing regulations for the medical device remanufacturing (also
RAPS: FDA to Implement All COVID-19-Related Guidance Immediately, Without Public Comment
In light of the need to act quickly and efficiently to respond to the COVID-19 public health emergency, the US Food and Drug Administration (FDA) on Friday said that it anticipates that prior public participation
The man behind NZ’s sustainable healthcare start-up talks business
His idea to reprocess used medical devices is already helping reduce waste in the New Zealand healthcare sector. Now Oliver Hunt of Medsalv discusses plans for the future and what’s needed for a small business
Unlocking Healthcare Cost Savings from Medical Devices: Industry’s Untapped Value Vault
Americans spend more on healthcare than anyone else in the world. Although the high cost of prescription drugs are often thought of as a primary driver – and make no mistake, Americans spend double the
HCWH: A New Road Map for Strategic Procurement in European Healthcare
Thanks to Health Care Without Harm, EU-based hospitals and national health systems have a new roadmap to strategic procurement. The Association of Medical Device Reprocessors, or AMDR, hopes EU hospital leadership will spend time reviewing Health