About this event
Navigating the complexities of 510(k) submissions can be overwhelming for medical device manufacturers. Join NPG for an insightful webinar where our industry veterans will share their expertise on how effective regulatory project management can streamline your submission process, reduce time-to-market, and increase your chances of approval.
You’ll hear real-world examples of successfully managed projects, highlighting how strategic project management enhances compliance, streamlines processes, and ensures seamless collaboration. Attendees will gain actionable insights into mitigating risks, accelerating timelines, and focusing on innovation with the right project management support.
What You'll Learn:
Who Should Attend:
This webinar is designed for Directors, VPs, and key decision-makers in the medical device industry who are responsible for 510(k) submissions and who seek to navigate the regulatory process successfully.
Network Partners Group (NPG) is a leading life sciences consulting firm serving in the medical device, pharmaceutical, and biotech industries. NPG has five Centers of Excellence, specializing in labeling, packaging engineering, quality, regulatory affairs, and project management.
