Journal2016-08-10T08:51:55-04:00

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

AMDR Presents at CleanMed Europe 2016

CleanMed Europe 2016 – Day 3 Round-Up   The final day of CleanMed Europe 2016 featured a wide range of parallel sessions where participants shared ideas and best practices on a wide range of topics including

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