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In 2025, refining product development and manufacturing strategies is essential to stay competitive in the evolving life sciences and medical device market. With new regulatory requirements and rising expectations for product quality, finding ways to reduce risk and accelerate time-to-market is even more challenging. Your competitors are finding new ways to deliver speed and profitability—don’t get left behind.
Gain key insights to achieving profitability, avoiding manufacturing challenges, and taking advantage of the latest innovation to exceed your goals. Learn from a panel of experts who have launched hundreds of medical instruments and devices for both start-ups and Fortune 100 companies.
Key Takeaways:
Speakers:
Steve Laninga, Managing Director, Medical Devices
Joe Wong, Director, R&D
Pete Oberst, Director, Applications
Amy Parker, Director, Quality & Compliance
Ray Kime, SVP Operations