Special Offer 2017 for Medical Devices Webinar Attendees! ONLY $10 each

[John Robinson]

$10 can buy you many items of daily user. These items serve their purpose: Once you’ve finished using them, you buy them again. Have you heard about a special offer in which you gain unlimited knowledge with which you scale up in your profession?

Yes, this is the kind of special offer that GlobalCompliancePanel, a leading provider of professional trainings for the regulatory compliance industries, has for you! For 2017, make the most of this special offer for medical devices webinars. By enrolling for any of these webinars and attending them by playing them for an unlimited number of times for up to six months; you fill the gaps in your profession that are preventing you from growing further.

If the high price of these trainings were a constraining factor all these years, leave those concerns behind. Under this special 2017 offer for medical device webinars from GlobalCompliancePanel; all that it costs to enroll for a webinar of your choice is a paltry $10!

And did you think the choice of topics is limited and commensurate with this small price?  No. In fact, it is inversely proportionate: You have something like 500 and more webinars to choose from! Isn’t this what you call an offer and a surprise of a lifetime? GlobalCompliancePanel makes this possible. Why pay the original price of $265 when you can buy these webinars for $10?

With such a huge collection of recorded webinars to choose from, why not take a look at some of them:

Our expert, Kosta Makrodimitris, Biomedical/Health Informatics Advisor, Author & Strategist, will explain what you need to understand in order to implement the FDA’s 2012 Rule which requires that most medical devices distributed in the US carry a unique device identifier (UDI) with the intention of improving the quality of information about medical devices and to improve traceability in the event of a disaster. This webinar will explain the complete details of this Rule and give you an understanding of how to identify problems with the product more easily and quickly.

Medical device Design Control is a major aspect of this industry, as professionals like you are aware. The regulatory and quality requirements of Design Control will be explained at this webinar. You can use this understanding to implement better Design Controls in your medical devices and to satisfy regulatory requirements.

What are you waiting for? Don’t let go of a rare opportunity such as this!

Contact Details:

https://www.globalcompliancepanel.com/webinars_home?medtechiq-2017-SEO

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