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In medical device manufacturing, success means staying abreast of regulatory changes from Argentina to the United Kingdom ... and beyond.
Impossible? Not at all. Here’s how:
Announcing publication of the 2013 edition of the ...
FDAnews Guide to International Medical Device Regulation
It’s the one-stop authority for quick, accurate answers to all your questions on:
International compliance is no longer simply a matter of following the same old rules. Enforcement activities and practices are changing. Countries are beginning to share data about manufacturing firms, increase the number of inspections, and crack down on issues such as counterfeiting and improper marketing. You learn the new rules of the game, or cede the playing field to competitors.
That’s where the FDAnews Guide to International Medical Device Regulation: 2013 Edition comes in. Our editors monitor and report on regulatory developments affecting device production in more than 45 nations around the world. They’ve compiled more than 150 reports highlighting changes from the past year that could supercharge your international sales ... or stop them in their tracks.
You’ll turn to this total regulatory reference time and again in the months ahead. It will become your one-stop source for:
To compete internationally, you must comply internationally. It’s a lesson your competitors have learned. Don’t get left behind. Place your advance order now.
FDAnews Guide to International Medical Device Regulation: 2013 Edition is published in print and CD format.
Get Multi-user Access With The Electronic Books Library.
Save money with a license agreement allowing significant numbers of users access to an electronic version of this book. For multi-user access to multiple titles, FDAnews offers the Electronic Books Library – a personalized collection of FDAnews publications that is fully searchable. Contact customer service for a quote or more information.
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