Stay Ahead of Evolving Regulations with AI-Driven Compliance
Regulatory requirements across the Life Sciences and MedTech industry are becoming increasingly complex. From FDA, EU MDR, and IVDR to EUDAMED and emerging global regulations, organizations are expected to maintain continuous compliance while accelerating innovation, product launches, and market access. Yet many organizations continue to rely on fragmented systems, manual evidence collection, siloed supplier information, and disconnected compliance processes—resulting in audit risks, increased operational costs, delayed submissions, and slower time-to-market. Join Birlasoft and Certivo for an exclusive executive Panel Discussion to discover how AI-powered compliance can transform regulatory operations from a reactive function into a strategic business advantage.
Featured Speakers
David Bartlett
Vice President – Digital Strategy Practice
Birlasoft
Vice President – Digital Strategy Practice
Birlasoft
David leads enterprise digital transformation initiatives that enable Life Sciences organizations to modernize operations through connected platforms, AI, automation, and intelligent compliance strategies.
Kunal Chopra
CEO, Certivo
Birlasoft
CEO, Certivo
Birlasoft
Kunal brings deep expertise in AI-powered regulatory intelligence, automated evidence management, and digital compliance solutions that help organizations simplify complex regulatory processes.
John LaLonde
MedTech Industry Expert
MedTech Industry Expert
John has extensive experience helping global MedTech organizations navigate regulatory requirements, accelerate market access, and address practical compliance challenges throughout the product lifecycle.
During this Panel Discussion, our experts will demonstrate how an intelligent, AI-powered compliance ecosystem can help organizations:
Key Discussion Topics
- Navigating FDA, EU MDR, IVDR, EUDAMED, and evolving global regulations.
- AI-powered regulatory intelligence and continuous monitoring.
- Connected GxP compliance across enterprise systems.
- Supplier evidence automation and digital quality management.
- Technical file readiness and submission acceleration.
- AI-enabled audit readiness and enterprise compliance visibility.
- Future-proofing regulatory operations through intelligent automation.
Why Attend?
- CFOs & Risk Leaders - Reduce financial exposure from non-compliance, product delays, remediation efforts, and regulatory penalties while improving governance and operational resilience.
- COOs & Manufacturing Leaders - Embed compliance into manufacturing and operational workflows without increasing complexity, manual effort, or headcount.
- Regulatory Affairs, Quality & Compliance Teams - Improve submission readiness, strengthen audit confidence, enhance traceability, and reduce manual compliance activities.
- Engineering & Product Development Leaders - Integrate compliance earlier into product design, engineering, change management, and product lifecycle processes.
- Supply Chain Leaders - Improve supplier collaboration, automate evidence collection, enhance supplier quality, and strengthen global regulatory readiness.
- CIOs & Digital Transformation Leaders - Connect enterprise systems to create a unified, AI-enabled compliance ecosystem that supports business agility and continuous regulatory readiness.
Register Today
Don't let regulatory complexity slow innovation. Discover how AI can help your organization move from reactive compliance management to continuous regulatory readiness and transform compliance into a competitive advantage. Reserve your seat today and learn how to build a connected, AI-powered GxP compliance ecosystem for the future of Life Sciences.
Date: Tue, Aug 18, 2026
Time: 11:00 AM - 12:00 PM EDT