FMMC Florida Medical Device Symposium
Welcome FMMC Symposium Attendees!
QualityHub is proud to be part of the 19th Annual Medical Device Symposium. Whether you’re joining today for expert-led sessions, networking with industry peers, or exploring the latest in regulatory and quality innovation, we’re glad you’re here.
Our on-site QHub Team is committed to helping medical device companies managecomplexity, strengthen compliance, and build sustainable quality systems. If you see a Team Member, stop and have a chat!
While you’re here, we invite you to explore exclusive resources and insights created specificallyby QualityHub for symposium attendees.
Sean Boyd
Corporate Vice President, QualityHub
Wednesday, May 6
1-2:20 pm EST
FDA SUPER SESSION: Agency Priorities, QMSR Implementation & FDA’s New Inspection Model
Gain clarity on the FDA’s evolving expectations, how QMSR impacts your organization, and what the new inspection model means for your readiness strategy.
Rebecca Fuller Senior Vice President, Regulatory Compliance, QualityHub
SPECIAL WORKSHOP: Envisioning Risk as a “System”: Driving Risk-Based Decisions Across the QMS and Product Lifecycle
Program Note: Due to unforeseen circumstances, QualityHub’s in-person Special Workshop “Envisioning Risk as a ‘System’: Driving Risk-Based Decisions Across the QMS and Product Lifecycle” will no longer take place as scheduled. QualityHub will instead offer this session in a virtual format at a later date.
Exclusive Attendee Resources
Take advantage of curated materials designed to extend your learning:
Expert White Paper: Building a Culture of Quality
Explore strategies for embedding quality into every layer of your organization.
QHub Insights Newsletter
Stay informed with the latest regulatory updates, trends, and expert perspectives.
How QualityHub Supports Your Company’s Success
QualityHub partners with life sciences organizations to solve complex challenges across the product lifecycle.
Our services include:
Quality Systems Auditing
Objective, thorough assessments to ensure compliance and readiness.
FDA Inspection Support
Preparation, real-time support, and post-inspection remediation guidance.
Compliance Remediation
Strategic recovery plans to address gaps and restore confidence.
Quality Systems Training
Practical, role-based training that strengthens your internal capabilities.
QMS Consulting
Design, implementation, and optimization of scalable quality systems.
Clinical Consulting
Support for clinical strategy, execution, and compliance.
Regulatory Compliance Consulting
Navigate global regulations with confidence and clarity.
Product Development
Integrating quality and compliance from concept through commercialization.
Project Management
Driving timelines, alignment, and execution across critical initiatives.
Risk Management
Embedding proactive, system-level risk thinking into your organization.