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EU MDR vs. US FDA 510(k): Navigating Key Differences in Medical Device Regulations

EU MDR vs. US FDA 510(k): Navigating Key Differences in Medical Device Regulations

EU MDR vs. US FDA 510(k): Navigating Key Differences in Medical Device Regulations

The global medical device market is governed by stringent regulatory frameworks that ensure patient safety and device efficacy. Two of...

Oct 8, 20243 min read

Balancing Innovation & Ethics: The Race for Effective AI Regulation Across the Globe!

Balancing Innovation & Ethics: The Race for Effective AI Regulation Across the Globe!

Balancing Innovation & Ethics: The Race for Effective AI Regulation Across the Globe!

Introduction Artificial Intelligence (AI) is rapidly transforming industries, enhancing productivity, and shaping the future of human...

Oct 8, 20244 min read

Best Practices for Post-Market Surveillance in Medical Devices

Best Practices for Post-Market Surveillance in Medical Devices

Best Practices for Post-Market Surveillance in Medical Devices

The medical device industry is dynamic and heavily regulated to ensure patient safety and product efficacy. Once a medical device reaches...

Oct 8, 20243 min read

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