Insights & Events
Quroba hosts events and creates useful materials we hope will help you navigate your compliance journey.
Insights
Learn about Quroba and recent activitiesBringing 25 Years of Regulatory Expertise to Every Team—with a Powerful Suite of AI Tools
Simplifying Compliance in Medtech, Biotech, and Digital Health Through Expert-trained AI Tools
May 19, 2025 12pm PDT / 3pm EDTRead Now
Cancer Disparities in Women's Health: Barriers, Advances, and Equity
Closing The Gap in Cancer Care Through Equity and Access
February 28, 2025 12pm PDT / 3pm EDTRead Now
The Rise of Fem-Tech: How New Tools Are Changing Women's Health
Bridging Technology and Access in Women's Health
February 14, 2025 12pm PDT / 3pm EDTRead Now
The FDA's Evolving Stance on AI Algorithms: Balancing Innovation with Safety
Balancing Innovation and Oversight in AI-Driven Healthcare
December 12, 2024 12pm PDT / 3pm EDTRead Now
East Asia's Rising Influence in 510(k) Clearances: Trends, Challenges, and Competitive Edge
International Progress in Navigating Regulation to Drive Innovation
November 19, 2024 12pm PDT / 3pm EDTRead Now
Regulatory Strategy in Cardiac Medical Devices: The Role of AI, SaMD, and Cybersecurity
A New Era for Cardiac Medical Device Innovation and Compliance
October 17, 2024 12pm PDT / 3pm EDTRead Now
FDA Expands PCCP Guidance For AI Medical Devices
A Game-Changer for Developers and AI Medical Devices
September 14, 2024 12pm PDT / 3pm EDTRead Now
Past Events + Resources
Watch Past WebinarsQuroba Conversations
Artificial Intelligence and Machine Learning in MedTech
November 15th, 12pm PDT / 3PM EDTWatch Now
Quroba Conversations
Quroba Conversation: Clinical Validation and Efficacy: The Patient
October 17th, 12pm PDT / 3pm EDTWatch Now
Quroba Conversations
Quroba & AccurKardia discuss FDA clearances
September 12th, 12pm PDT / 3pm EDTWatch Now
Quroba Conversations
Quality Management Systems Overview (ISO 13485 / US FDA 21 CFR Parts 820/830)
August 1st, 12pm PDT / 3pm EDTWatch Now
Quroba Conversations
Overview of FDA process: from pre-sub to approval
June 20th, 12pm PDT / 3pm EDTWatch Now