AMDR Welcomes the Pan American Health Organization and INVIMA to Hygia
AMDR welcomes the Pan American Health Organization and INVIMA, the Colombian Medical Product competent authority to Hygia! We look forward to cooperating as PAHO contemplates a comprehensive, Pan American medical
Interview: Where Do New Reprocessing Rules Leave EU?
Questions over proper oversight and allowances for reprocessing of single-use devices in the EU caused significant debate among policymakers who developed the pending European Medical Devices Regulation. Reprocessing advocate Dan Vukelich talked
Association Between Surgeon Scorecard Use and Lower Operating Room Costs
Source: HPN Online Despite the significant contribution of surgical spending to healthcare costs, most surgeons are unaware of their operating room (OR) costs. A study published in JAMA Surgery looked at the association
South Africa, Department of Health, Medicines and Related Substances Act, Regulations Relating to Medical Devices and In Vitro Medical Devices (9 December 2016)
“…’manufacture’ means operations that include the design, purchasing of material, specification development, production, fabrication, assembly, processing, reprocessing, releasing, packaging, repackaging, labelling, and refurbishing of a medical device or IVD, as the case may be, and
Good As New – Reprocessing Single-Use Devices
Source: Medical Device Developments There are many challenges to pre-hospital sterilisation methods of medical equipment, from single-use disposable devices to longer-lasting equipment designed to work for years. Kerry Taylor-Smith explores the ongoing debate around reprocessing single-use
Reprocessed Medical Devices Market Expected to Surpass $5 Billion by 2023
A new report by Global Market Insights forecasts that revenue from the reprocessed medical device market will increase by 20% CAGR by 2023, growing from $1.12 billion to over $5 billion. "Based on the type of product,