Now! For the First Time
Every moment of every day, countries around the globe are changing the rules on medical devices and diagnostics. Product applications and marketing authorizations … postmarket testing and safety monitoring … manufacturing quality, recalls and complaints reporting … streamlined approvals processes in some cases, more complex processes in others. There’s so much to keep track of – and so little time.
Introducing International Devices & Diagnostics Monitor (IDDM) the new one-stop resource that brings you a complete, global picture of the medical device regulations that affect your business.
Nowhere else will you find a more comprehensive collection of all the regulatory changes in the US, EU, Asia, Latin America, the Middle East, Australia and the rest of the world.
Your subscription includes a weekly newsletter to keep you up to date with global regulations as they happen.
In addition, you will also receive a quarterly update with expert analysis on key device and diagnostic issues from around the world. Most importantly, you'll have access to a website completely dedicated to global medical device regulations, www.IDDMonitor.com.
With International Devices & Diagnostics Monitor, you won't miss a thing. You'll be fully prepared with an unmatched source of critical information and news, including:
Could you track these global changes yourself? Perhaps – at the cost of countless hours. Why even try? FDAnews is doing the job for you, at a fraction of what it would cost to do it yourself.
So don’t waste another instant. Start your NO-RISK subscription to IDDM NOW