International Medical Device Regulatory Monitor (IMDRM) tracks all the relevant topics – from clinical trials and listing requirements to marketing and manufacturing regulations – in the markets where you need to stay compliant. Our editors track long-established regulatory leaders, such as the EU, Japan and the U.S; important, fast-growing markets, such as Brazil, Russia, India and China; and smaller markets that are gradually strengthening their regulatory structure, such as the Middle Eastern nations.
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