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SUMMARY:Global MedTech Regulatory Trends: True Quality Summit Series
DESCRIPTION:Watch Live: August 30-September 1\nThen available on-demand \nMedTech regulations are evolving. Increasing globally\, changing constantly\, creating headaches for you and medical device companies around the world. It’s your responsibility to assess the changes unfolding to fully understand the impact on your business and product. \nAre you ready to adapt? \nTo help you navigate the changing regulatory landscape\, we’ll be taking you on a tour around the world\, diving into the state of regulations\, upcoming critical events\, and what you can expect in the future during the Global MedTech Regulatory Trends: True Quality Summit Series \nOn August 31st\, at 10AM\, watch our very own Carrie Hetrick\, Sterling’s Director of Regulatory and Clinical Affairs present “How Regulatory Changes can Impact Product Development.”  \nHERE’S WHAT YOU CAN EXPECT AUGUST 30TH-SEPTEMBER 1ST: \n\n\nEngaging sessions around Brexit/Swexit\, UDI\, MDSAP\, QMSR Harmonization\, EU IVDR\, and more!\nLearn from speakers with expertise and insights in each region — from Israel to Latin America\, to APAC\, to EMEA and North America.\nDiscover key deadlines\, updates\, and dealbreakers that are necessary for you to get (and keep) your devices on the market\nLearn how to stay ahead of the ever-evolving changes and trends in the industry\nChoose your own adventure across 15 sessions\, ask live questions\, and get instant access to hours of on-demand recordings when the event is over\n\nRegister Now \nEngage with us on social media using #GlobalMedTechSummit
URL:https://www.vantagealm.com/event/global-medtech-regulatory-trends-true-quality-summit-series/
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