True Quality Virtual Summit: Global Medical Device Regulatory Updates
By Anne Holland
CEO, QA Consulting, Inc.
MedTech 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.
Are you ready to adapt?
As a Greenlight Guru partner, QA Consulting invites you to attend the Global MedTech Regulatory Trends: True Quality Summit Series Aug 30-Sept 1. The free, three-day event features industry experts who will guide you through various regulations from each major region, and where they’re headed for the future.
MedTech professionals assembled by Greenlight Guru will help you navigate the changing regulatory landscape, 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.
Here’s What to Expect
- Engaging sessions around Brexit/Swexit, UDI, MDSAP, QMSR Harmonization, EU IVDR, and more!
- Learn from speakers with expertise and insights in each region — from Israel to Latin America, to APAC, to EMEA and North America.
- Discover key deadlines, updates, and deal breakers that are necessary for you to get (and keep) your devices on the market.
- Learn how to stay ahead of the ever-evolving changes and trends in the industry.
- Choose your own adventure across 15 sessions, ask live questions, and get instant access to hours of on-demand recordings when the event is over.
Watch this Space
I’ll be attending the summit and will be posting my key takeaways here on the QA Consulting Blog. It’s sure to be an information-packed event. I’d like to hear from you and get your thoughts or questions. If you attend, please drop me a line on our Contact Page.
QA Consulting is a partner with Greenlight Guru. Together, we provide medical device-specific solutions that accelerate the delivery of life-changing devices. Greenlight Guru’s Medical Device Success Platform coincides with QA Consulting’s deep expertise in developing strategies for medical device regulatory and quality success.