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Tag: medical device

Guidance Reveals How NMPA Inspects Your Clinical Trial Institution

NMPA announced the “Measures for Supervision and Inspection of Medical Device Clinical Trial Institutions (Trial)” on March 12, 2024, for feedback, along with the...

How Post-Market Surveillance Enhances Medical Device Safety

Understanding Post-Market Surveillance:In the fast-paced world of medical technology, the journey of a medical device doesn’t end with regulatory approval. It continues into the...

Asensus Surgical, Inc. Schedules Fourth Quarter and Full Year 2023 Financial and Operating Results Conference Call for March 21, 2024 | BioSpace

RESEARCH TRIANGLE PARK, N.C., March 15, 2024 (GLOBE NEWSWIRE) -- Asensus Surgical, Inc. (NYSE American: ASXC), a medical device company that is digitizing the...

DRAP Draft Guidance on Clinical Research: Final Reporting | Pakistan

The new article describes the approach to be applied concerning reporting and record-keeping in the context of clinical investigations associated with medical devices intended...

Health Canada Guidance on Medical Device Recalls: Overview | RegDesk

The article highlights the critical points related to the recall procedures applicable to medical devices allowed for marketing and use in Canada. ...

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