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Medical Device

TMDA Released Guidance on the Import of Research Products to Be Used in Clinical Research

Europe: Medical Device Incident Reporting

China’s CMDE Announces New Regulations on the Supervision and Administration of Customized Medical Devices for Clinical Trials

An Overview of European Unique Device Identification System

Medical Device Post Market Surveillance

Why is Medical Technology Getting Shrouded by the Fear of Cybersecurity Issues?

The First Step

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