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.
PLUS, in every issue, you get links to additional key documents from international agencies and commissions that support IMDRM’s articles, such as guidances, warning letters, rules, full texts of proposed legislation, regulations, papers, presentations, and more.
With your subscription you’ll also receive:
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Bonus, order today and get a free copy of our best-selling webinar - Newly Proposed EU Medical Device Regs Understanding the 7 Big Changes That Could Impact Your Device.
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Monthly, 12 issues/year
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