We're going to San Diego to learn, connect, and find inspiration at the must-attend experience for MedTech professionals who drive innovation in the market today.
True Quality 2022, presented by Greenlight Guru, will be in San Diego for emerging medical device companies, strategic partners and medical device industry thought leaders.
Whether you're a CEO looking to grow faster or navigate a new market, or a young QA/RA professional learning to master and execute closed-loop traceability, there’s a seat at the table for you.
Through educational sessions, intentional networking, and engaging activities the status quo of treating compliance as a checkbox activity will disappear and medical device leaders will emerge, connect, and gain inspiration.
The regulatory pathways you choose to pursue will be a major influence on your go-to-market strategy. But navigating these pathways, especially in the two largest markets for medical devices—the US and the EU—, can quickly become complicated. During this session, you’ll learn about the nuances, similarities, and differences of regulatory pathways in the US, EU, and other markets. Join regulatory experts from both sides of the Atlantic to discover how timelines, costs, and other considerations can affect the complex questions of which markets to pursue and when to make your move.
Come listen to Isabella, Schmitt, our Director of Regulatory Affairs perspective for this discussion that is critical knowledge for emerging medical device companies.
Check out the event agenda, here.
Contact us at Hello@ProximaCRO.com asking to book a meeting with our team at this conference.
Look for our superhero, Proxi!
