Enabling you to identify and mitigate the intrinsic risk in your operations, supply chains and business processes.
Evaluating how your products and services meet and exceed quality, safety, sustainability and performance standards.
Validating the specifications, value and safety of your raw materials, products and assets.
As you map out your global strategy beyond the North America and Europe, there are six key steps to follow and multiple regulations to consider. Harmonization has increased in recent years, yet most countries still maintain distinct medical device regulatory systems. This webinar will explore these six steps and reveal insights into the unique medical device regulations affecting five of the largest and most rapidly-growing global markets – Brazil, Russia, India, China, and Japan -- an important and powerful block of nations also known as the ‘BRIC Countries + Japan.’
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