If you’re involved in medical device packaging, you’ve got a lot of support these days, with even more on the way. The latest revision of ISO 11607-1/2: 2019, “Packaging for terminally sterilized ...

The medical device sector must meet stringent regulatory requirements plus convince potential customers that they make reliable, safe products. Having a strong commitment to quality can help customers ...

Medical device companies MUST have established risk management processes that comply with ISO 14971. And it doesn’t matter if you are developing medical devices in the U.S., EU, Canada, and so on. ISO ...

Over the last 15 years, ISO 10993-18 has become a notable resource for professionals at each stage in the supply chain and manufacturing of medical devices, assisting them in the evaluation of ...

Elayne Gordonov, Market Manager - Global Bio Market at Instron, talks to AZoM about physical testing requirements of syringes, Luer connections, and needle-based injection systems in-line with ISO ...

MANILA, Philippines - On March 27, 2009, the National Kidney and Transplant Institute (NKTI) Medical Laboratory made a significant milestone in the history of diagnostic medicine in the country as it ...

McCormick Industries today announced expanded emphasis on ISO 9001:2015-certified processes supporting its precision CNC medical machining services, underscoring the organization’s commitment to ...