Event focus: Medical devices are growing in numbers and complexity. Much is being done towards examining potential changes to submissions and reporting requirements to ensure device safety and efficiency of new and existing products. In addition, medical device manufacturers are facing demands for innovation, compliance with strict and evolving rules, and shrinking premiums, not to mention intense competition, which also require faster times to market. Strategic features: > Design for continuous safety improvement > Comprehension and compliance regarding latest regulatory and global requirements > Consideration of human factors engineering in safety equation > Alignment of corrective measures to strategic planning for cost-effective and timely

Date : 22nd January 2015 to 23rd January 2015

Place : United States, Las vegas

Website :http://pharma.americanleaders.com/medical-device-safety-conference-201501?utm_source=All%20Conference%20Alerts&utm_medium=listing&utm_campaign=ALLS13home

Contact Person:Francesco Toscano

Description:

Event focus: Medical devices are growing in numbers and complexity. Much is being done towards examining potential changes to submissions and reporting requirements to ensure device safety and efficiency of new and existing products. In addition, medical device manufacturers are facing demands for innovation, compliance with strict and evolving rules, and shrinking premiums, not to mention intense competition, which also require faster times to market. Strategic features: > Design for continuous safety improvement > Comprehension and compliance regarding latest regulatory and global requirements > Consideration of human factors engineering in safety equation > Alignment of corrective measures to strategic planning for cost-effective and timely

Event focus: Medical devices are growing in numbers and complexity. Much is being done towards examining potential changes to submissions and reporting requirements to ensure device safety and efficiency of new and existing products. In addition, medical device manufacturers are facing demands for innovation, compliance with strict and evolving rules, and shrinking premiums, not to mention intense competition, which also require faster times to market. Strategic features: > Design for continuous safety improvement > Comprehension and compliance regarding latest regulatory and global requirements > Consideration of human factors engineering in safety equation > Alignment of corrective measures to strategic planning for cost-effective and timely will be held in Las vegas,United States on date 2015-01-23

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Deadline for abstracts/proposals : 21st January 2015

Keynote Speakers :

Check the event website for more details.