With contributions from more than 30 international experts, this new loose-leaf manual shows you how to satisfy all European regulations affecting your medical devices.
You’ll find clear, practical and up-to-date guidance for every class of medical device and at every stage in the product life cycle, from selecting your conformity assessment route to registering with a competent authority and complying with global harmonization.
Plus, your guidance stays up to date. The Medical Devices Manual includes a free annual update plus two free supplements. Subsequent updates and supplements will be available each year so you’re always working with the right information and the best regulatory strategies.
Order today and you can fast-track your entry into European markets with easier, surer compliance through directives affecting every aspect of business, including:
Put top consultants to work for your future. In developing the Medical Devices Manual, Euromed Communications draws on more than 30 leading experts on medical device requirements in the UK, France, Italy, Germany and other European Union countries.
Meet the Publisher
Established in 1993, Euromed Communications has a core of qualified professionals supplemented by a team of expert medical and scientific researchers. The company produces publications for the scientific community inexpensively, accurately and rapidly.
With more than $100 million at stake in Europe’s medical devices markets, your competitors won’t wait for you to get up to speed on regulations. Click here to order your manual now!
Medical Devices Manual is available in loose-leaf format for $592. Price includes loose-leaf manual, one free update and two supplements throughout the year.
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