Roundtable Discussion: Building out a Software Bill of Materials for Embedded Packages, Open Source & Third-Party Software to Meet FDA Requirements & Ensure Regulatory Approval
Time: 2:30 pm
day: Day One
Details:
- Addressing the vague regulatory expectations regarding the quantity of tangible elements required in the software Bill of Materials, and exploring strategies to meet these expectations without compromising efficiency
- Clarifying FDA expectations on showcasing direct and/or transitive dependencies within software composition analysis, with a focus on identifying the optimal levels of dependencies needed to satisfy regulatory requirements and ensure efficient use of time and talent
- Exploring the intricacies of vulnerability scans in the assessment of vulnerabilities in open source and third-party software packages
