CyberMed
Invite-Only RA/QA Consultant Roundtable

Align regulatory, quality, and cybersecurity counsel for 2025.

CyberMed convenes trusted RA/QA advisors to swap insights, harmonize playbooks, and anticipate reviewer questions that intersect security and quality requirements.

Thursday, November 21 • 2:00 PM ET
Invite only
Virtual (Zoom)
Request an invite
Roundtable recap coming soon

Agenda highlights

Expect an interactive roundtable—no slide decks. Each topic includes collaborative canvases that you can reuse with your clients after the session.

  • Coordinating RA/QA and security commitmentsShare frameworks for aligning remediation timelines, supplier controls, and submission narratives across consulting teams.
  • Regulatory intelligence exchangeCompare notes on FDA AI/ML discussion papers, MDCG updates, and how clients are responding in quality systems.
  • War room simulationWe'll run through a mock adverse event and walk out with a shared escalation playbook for consultants.
  • Roundtable insightsOpen mic for participants to surface trends, tooling, and collaboration ideas for the new year.

Who should request an invite?

Regulatory strategists, quality leaders, and fractional executives who advise medical device manufacturers on commercialization and compliance, and who want to integrate cybersecurity expertise into their counsel.