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5th Annual Medical Device Global Regulatory Intelligence Conference



 
Our Price: $495.00

Product Code: 2276
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About the Product
Includes presentation materials from the conference. Presentations slides are in PDF. format. All files are available for immediate download.


About the 5th Annual Medical Device Global Regulatory Intelligence Conference:

Maintaining Regulatory Compliance throughout the Medical Device Product Lifecycle, from Ensuring Global Product Clearance through Appropriate Clinical Data & Post-Market Surveillance, to the Implementation of UDI Requirements on a Worldwide Scale, all while Evolving with Worldwide Regulatory Frameworks


Given the dramatic increase in the number and complexity of medical device technologies on the market today, regulators have turned a closer eye towards this highly innovative industry, providing additional regulatory frameworks to ensure product safety and to mitigate risks. On a global scale, governments are increasingly adding to the regulatory burden for medical device manufacturers, resulting in regulatory teams that must continually evolve alongside changing regulatory targets and systems. Regulatory executives are looking for an opportunity to come together as an industry in order to discuss and debate global regulatory systems with a goal of maintaining abreast of the continually changing regulatory landscape facing medical device innovators today.

The 5th Annual Q1 Medical Device Global Regulatory Intelligence Conference provided attendees a highly customizable opportunity to engage and exchange knowledge with a wide variety of presenters on a tremendous number of medical device-specific topics. With multiple modules based on varied levels of knowledge or stage of implementation, attendees will have an opportunity to engage on the most important topics at that very moment, at the appropriate skill level. From UDI implementation and gauging the success of global UDI initiatives to rolling out UDI for Class II products, to an exploration of the changing dynamic in Europe due to the impending MDR, to case studies on Chinese and Russian markets, this program will provide a one-stop regulatory knowledge goldmine.



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