From Regulatory Uncertainty to Expertise

SBOM, CVE, and Beyond: Your Roadmap to Medical Compliance Confidence and Brand Protection

Thu, Jan 04, 2024 at 12 PM US Eastern /
6 PM EU Central / 9:30 PM India Standard

Can’t make the webinar? Register and we’ll send you a recording of it afterwards!

Are Overwhelming Compliance Processes Hindering Your Brand's Potential?

Join our webinar designed specially for medical device manufacturers and developers to help you achieve business growth through streamlined compliance, gain confidence in navigating new regulatory requirements, and protect your brand's integrity.

In this webinar, you’ll explore SBOM and CVE management and discover how to keep your products and devices compliant without complicating your development process. Say goodbye to complicated and unruly compliance processes and hello to efficient compliance practices that drive business growth! Your path to compliance clarity starts here!

 

What will you achieve with this webinar?

  • Gain confidence in compliance practices.
  • Simplify SBOM and CVE management.
  • Protect your brand's integrity.
  • Achieve business growth through compliance.
  • Overcome the belief that compliance is overwhelming.
  • Learn practical strategies for efficient compliance.
  • Connect with experts in the field.
  • Discover the value of compliance in your industry.
  • Transform compliance from a burden into an asset.

Additional Resources You'll Get in this Webinar Recording

COPY OF WEBINAR PRESENTATION

To quickly bring your team up-to-speed on new regulations for medical devices and best practices for becoming complaint

COMPLETE Q & A DOCUMENT

Centralizing the questions everyone is asking for your team to reference and get up to speed on the tools and resources the experts are using

SELF-ASSESSMENT CHECKLIST

To help you determine what gaps need to be addressed in your process so you can streamline meeting compliance regulations

CAN'T MAKE THE WEBINAR?

Register below and we'll send you a recoding of the webinar afterwards, along with the above additional resources!

THIS WEBINAR IS PART OF OUR "FROM REGULATORY UNCERTAINTY TO EXPERTISE" SERIES FOR MEDICAL DEVICE DEVELOPERS

The next webinar in this series will focus on post-market monitoring and he held on Thursday, Jan.04th