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Revolutionizing Complaint Management in Medical Device with AI-Integrated Quality Management Software

Dot Compliance

Introduction: In the fast-evolving landscape of the medical device industry, ensuring the highest quality standards is paramount. In this blog post, we will explore the benefits of using AI-integrated QMS for complaint management.

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2023 Deadline for Physicians, Advanced Practice Providers and Teaching Hospitals to Review Sunshine Act Data Approaching

Hall Render

Track – Physicians, advanced practice providers, and teaching hospitals should track all interactions with the pharmaceutical and medical device industry involving payments or transfers of value to ensure the accuracy of data reported in the Open Payments system on an annual basis.

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FDA Guidance Shows a Regulatory Path Forward for Interoperable Devices

Exeed Regulatory Compliance

Market for interconnected medical devices is projected to grow but the regulatory pathway is still evolving. Medical device industry is changing fast! Technology is driving rapid innovation and medical devices are becoming more interconnected, and smart!

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7 Things to Know About the New AdvaMed Code Updates

Healthcare Law Blog

On March 18, 2022, AdvaMed announced updates to the Code of Ethics on Interactions with Health Care Professionals (“Code”), a voluntary code that provides medical technology companies with guidance on ethically compliant interactions and relationships with healthcare professionals. The changes will take effect on June 30, 2022.

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