Council and European Parliament Reach Political Agreement on Medical Devices and In Vitro Diagnostic Medical Device Regulations
Following the May 25th European trilogue meeting, a political agreement has been reached on medical devices and in vitro diagnostic medical devices regulations. The two regulations on medical devices and in vitro diagnostics include
Third-Party Reprocessing is a Smart Idea for Hospitals
Nancy Chobin, former Vice President of Sterile Processing for Barnabas Health System and a 34-year veteran of the sterile processing industry, provides Informa's Infection Control Today with a thorough and informative Q&A
Reprocessed Medical Devices Market Analysis By Product and End-use; Segment Forecasts to 2022
Grand View Research has released the following market analysis report on reprocessed medical devices: Reprocessed Medical Devices Market Analysis By Product (Cardiovascular Devices, Blood Pressure Cuffs, Positioning Devices, Cardiac Stabilization Devices, Diagnostic Electrophysiology Catheters, Deep
Greenhealth Magazine Announces Top Environmental Excellence Award Winners
Greenhealth Magazine, published by Practice Greenhealth, has announced the 2016 winners of the annual Environmental Excellence Awards. One significant factor in the selection process continues to be Environmentally Preferable Purchasing (EPP), the procurement of goods and
How Companies Can Do Well by Doing Good
How Companies Can Do Well by Doing Good Source: Sarah Begley, TIME Conventional wisdom holds that corporations are the enemy of the common good, willing to exploit workers and pollute the environment if it helps
United Kingdom, Medicines & Healthcare Products Regulatory Agency:
Single-Use Medical Devices: UK Guidance on Re-Manufacturing (2016) “…Single-use devices may be re-manufactured for use in the UK. However, the remanufacturer, prior to placing their device on the UK market or to putting it into