Informa Markets Engineering West, featuring MD&M West and other co-located shows, was the first large-scale trade show to return in-person in California. West+ will extend the educational opportunities with an encore virtual event.
ISO 13485 certification is an internationally recognized standard for medical device companies involved at any stage of a product’s lifecycle. Here are some of the many reasons why organizational leaders choose to get their companies certified.
FDA alerted patients, providers, and medtech manufacturers that cybersecurity vulnerabilities reported Tuesday by BlackBerry may affect certain medical devices. The company reportedly kept the software flaw secret for months.