International Medical Device Regulatory Monitor: Renew Now!

International Medical Device Regulatory Monitor

Renew International Medical Device Regulatory Monitor

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.

Renew today and continue to receive this valuable information.

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.

To Recap, Here's What Each Issue Provides:

  • Email Alerts. Each electronic issue will be delivered right to your email inbox;
  • Online Access. Search the current issue, plus 8 years of archives by keyword and relevancy;
  • Free Documents. Each issue contains up to 10 links to full text of hard-to-obtain key int’l medical device regulatory references, guidances, consensus standards and industry reports, and other primary source documents you need. Never waste time tracking documents again!
  • FDAnews Device Daily Bulletin. This daily email alert brings you important FDA and international regulatory, legislative and business news in the medical device industry.

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