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Given the recast of the European Medical Device Directive and the recent changes to the FDA's 510(k), the regulatory climate in the medical device industry is more volatile than ever. Medical Device manufacturers are concerned with staying up-to-date with these regulations, accelerating time to market, reducing cost and improving profit margins. Moreover, expanding into different markets within and outside Europe poses new issues – can you risk not being on top of the latest changes? Opal Events' Medical Devices Summit Europe will address these topics and help you prepare strategies to meet current and to anticipate incoming challenges.
Not sure if you want to exhibit at or attend the Medical Devices Summit Europe? See the panels below to get the information you need to make an informed decision.
|Conference/Event Dates:||11/11/2013 - 11/12/2013|
|Other Industries:||Manufacturing, Medical|
|Audience:||executives from medical device manufacturers; Vice Presidents, Directors, Managers, and Engineers of: Compliance, Quality, Regulatory Affairs, Software Engineering, Outsourcing, Supplier Management, Research & Development, Product Development, Commercial Operations|
|Venue:||Clyde Court Hotel|
|Venue Type:||Indoor - Hotel|
|Official Conference Hotel:||Clyde Court Hotel|
|Conference Hotel URL:||http://www.clydecourthotel.com/...|
|Show Manager:||Opal Events|
|Booth Size||Booth Cost||Available Amenities|
|Exhibiting is available.||Contact email@example.com for details.||Electricity:||Yes||- Unknown Price|
|Marketing Vehicles Allowed:||Call|
|Other Booth Sizes Available: n/a|
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