Knowledge Center

In an era defined by groundbreaking medical advancements, it's imperative for manufacturers to navigate the intricate regulatory landscapes of the European Union (EU) and the United States (USA) while harnessing strategic partnerships for expansion. We at Med-Di-Dia are thrilled to introduce a one-of-a-kind webinar meticulously crafted to equip medical device manufacturers with the insights, tools, and opportunities needed to thrive in these pivotal markets.

This webinar will provide Medical Device Manufacturers with

• An Opportunity to Unlock Regulatory Excellence: As medical device regulations continuously evolve, staying informed and compliant is paramount. Our webinar delves into the latest updates and nuances of regulatory frameworks in the EU and USA. From deciphering complex requirements to understanding approval processes, our experts will guide you through the maze, ensuring your path to market is not only successful but also streamlined.
• A Glimpse of Mentor, Ohio: Your Gateway to Success: Imagine a thriving hub strategically located to accelerate your medical device journey – Mentor, Ohio. With a dynamic blend of innovation, resources, and connectivity, this city offers a unique opportunity for manufacturers aiming to expand their presence. Our webinar unveils an exclusive chance to establish a strategic tie-up in Mentor, Ohio, leveraging its innovation ecosystem, skilled workforce, and conducive business environment.

Join us on Thursday 28^th September 2023 at

4:00 PM -5:00 PM (IST, UTC+01:00)

11:00 Am - 12:00 PM (EDT — Eastern Daylight Time)

Register now -  https://mailchi.mp/f40a0a3d319b/medtech-regulations-in-the-eu-and-usa

Drop your questions and queries by sending an email on mdd@mddltd.com