FDAnews Publication NEW Edition: Guide to International Medical Device Regulation — 2014 Edition

FDAnews’ 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 will keep devicemakers growing in international markets.

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Guide to International Medical Device Regulations: 2014 Edition

Guide to International Medical Device Regulations: 2014 Edition

Falls Church, VA (PRWEB) February 17, 2014

Guide to International Medical Device Regulation — 2014 Edition
**FDAnews Publication**
http://www.fdanews.com/IMDRM14

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 2014 edition of the Guide to International Medical Device Regulation

It’s the one-stop authority for quick, accurate answers to all questions on the fastest moving regulatory topics:

  •     New device regulatory frameworks in the EU, Japan and India
  •     Changes in inspection practices, including the single audit program
  •     Changes to quality manufacturing requirements
  •     New IMDRF standards
  •     Sunshine and transparency regulations
  •     UDI requirements
  •     Safety monitoring
  •     Computer programs embedded in devices
  •     Ever-changing registration requirements
  •     And dozens more key topics in device regulation worldwide

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. Devicemakers 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 — 2014 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 will keep devicemakers growing in international markets.

Readers will turn to this total regulatory reference time and again in the months ahead. It will become the one-stop source for:

  •     Coverage of the EU, Asia, Latin America, the Middle East, North America and Australia/Pacific
  •     Essential international regulatory changes from all of 2013
  •     Comprehensive summaries and explanations of the changes
  •     Key regulations – full-text printouts
  •     And much more!

To compete internationally, devicemakers must comply internationally. It’s a lesson the competitors have learned. Don’t get left behind.

Publication Details:
Guide to International Medical Device Regulation — 2014 Edition
**FDAnews Publication**
http://www.fdanews.com/IMDRM14

Format: Print or CD
Price: $387

Easy Ways to Order:
Online:     http://www.fdanews.com/IMDRM14
By phone: 888-838-5578 or 703-538-7600

About FDAnews:
FDAnews is the premier provider of domestic and international regulatory, legislative, and business news and information for executives in industries regulated by the US FDA and the European Medicines Agency. Pharmaceutical and medical device professionals rely on FDAnews' print and electronic newsletters, books and conferences to stay in compliance with international standards and the FDA's complex and ever-changing regulations.