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March 23, 2020

International Devices & Diagnostics Monitor

An FDAnews Newsletter

https://www.fdanews.com/IDDMLP2015

How helpful would it be to have a team of experts providing one with timely insights on all the global medical device regulations that specifically impact business?

Focus on complying with the latest requirements, ones resources management and maintaining profits while our dedicated, in-house group works on ones behalf to arm subscribers with a competitive edge by researching the U.S., EU, Asia, Latin America, the Middle East and Australia to share reliable, advance information, insights and news.

Subscribing to International Devices & Diagnostics Monitor (IDDM) is having this valuable in-house team, for a mere fraction of the cost, by your side.

The biweekly newsletter cuts through the noise to bring subscribers exactly what one needs to know, just when one needs to know it. Save time and money by knowing when — and how — to comply with changing global regulations.

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•Global medical device regulations

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IDDM’s compendium of facts and interpretation is delivered to subsribers with the complete text of relevant government documents, further saving you time and resources. One’s subscription includes special supplements (including warning letters and Form 483 inspection reports).

Our hand-picked subject matter experts and highly knowledgeable advisors create each issue so subsribers can benefit with actionable intelligence.

Start a one-year subscription (26 issues plus 24/7 access on devices.fdanews.com) to IDDM for only $1,247. Not bad for the equivalent of your very own, full-time research team.

Newsletter Details:

International Devices & Diagnostics Monitor

An FDAnews Newsletter

https://www.fdanews.com/IDDMLP2015

Subscription:

$1,247

Easy Ways to Subscribe:

Online: https://www.fdanews.com/IDDMLP2015

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

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