🧠 Topics

• One Submission, Many Markets: Mastering Regulatory Convergence — Thu, 28 Aug 2025

  Imagine a breakthrough MedTech innovation stuck in regulatory limbo—until you discover one submission that unlocks approvals across multiple markets. At QR Synergies’ webinar “One Submission, Many Markets: Mastering Regulatory Convergence,” you will learn how modular, LEGO-like dossiers and AI-powered intelligence streamline filings. Leverage IMDRF frameworks, pre-empt regulator queries, and slash redundant studies. Witness triumphs—a rapid PCR kit cleared by the FDA and CE in seven months, a smart inhaler approved across APAC and EU in five months, and an AI diagnostic app sailing through audits. Transform your strategy, accelerate approvals, and bring life-saving technologies to market faster. Register now!

• Med Align 360: Standardized Reporting for Medical Devices — Thu, 4 Sept 2025

  Join QR Synergies’ upcoming exclusive webinar series exploring Med Align 360: Standardized Reporting for Medical Devices and IVDs. In this 45-minute workshop, learn how top MedTech innovators integrate regulatory intelligence, harmonized QMS practices, and risk-based reporting to accelerate approvals and safeguard business continuity. Discover real-world case studies from Fortune 500 companies that highlight transformative wins—and costly pitfalls—when standardization is overlooked. Walk away with actionable frameworks aligned to ISO 13485, MDR/IVDR, and FDA requirements, plus a clear roadmap to reduce submission times by 40 % and nonconformances by 50 %. Don’t miss this unique opportunity to pioneer industry-leading reporting standards—reserve your spot now!

• One Size Fits One: Regulatory Routes in Personalized Devices — Thu, 11 Sept 2025

  Join QR Synergies’ webinar workshop and unlock the secrets to seamless personalized medical device approvals. Discover how to navigate IMDRF definitions, FDA custom and patient-matched pathways, global harmonization strategies, and integrated QMS frameworks to eliminate unexpected regulatory roadblocks. Learn from Fortune 500 MedTech case studies—3D-printed implants, patient-matched stents, rare disease IVDs—where risk management and strategic intelligence fuelled on-time global launches. Whether you’re a startup innovator or enterprise leader, walk away with a proven implementation roadmap and actionable KPIs that ensure uninterrupted market access, patient safety, and revenue continuity. Reserve your seat now to transform compliance chaos into predictable product rollouts.

• From Data to Deployment: Machine Learning Guidelines for MedTech — Thu, 18 Sept 2025

  Join our webinar series “From Data to Deployment: Machine Learning Guidance for MedTech” and unlock the roadmap to regulatory success. In this hands-on workshop, our expert will guide you through best practices in data management, risk-based quality systems, and SaMD lifecycle frameworks—anchored in major international regulations. Through real-world case studies, learn to implement Good Machine Learning Practices, conduct robust clinical evaluations, and establish adaptive algorithm governance that ensures compliance from concept to commercialization. Reserve your spot now to transform your AI-driven innovations into regulatory wins.

⏰ Webinar Schedule

We’re offering two time slots to ensure flexibility for global attendees.

👨‍💼 Your Trainers

Meet the Experts Who’ve Taken 100+ MedTech Devices to Market

• 30+ years in RA/QMS leadership
• Global strategic regulatory advocacy experts

👨‍💼👨‍💼 Who Should Attend

• MedTech Startups & Founders
• Regulatory Affairs Professionals
• Quality & Compliance Leads
• Medical Device Innovators & Exporters

📚 Format

• Training Duration: 45 minutes
• Interactive Q&A: 15 minutes
• Platform: Zoom
• Language: English

💳 Pricing

• India: ₹7,500 + Applicable Taxes per session
• International: $100 + Applicable Taxes per session

💬 Can’t make it live? No worries!

🎥 Lifetime access to session recordings + slides