As of late February, there were 147 medical device recall events and 20 of them, or 13.6%, were Class I, according to a Modern Healthcare report.

If you’re one of them or care for someone who is, the FDA recently updated a recall for more than 11,000 wheelchair devices meant to allow users greater ... now labelling the event as a Class I recall ...

a comprehensive understanding of the VAT refund process is essential for successful recovery. In 2024, the Ease of Paying Taxes (EoPT) Act introduced the new Risk-Based Approach in verifying and ...

The Medical Devices Compliance Program (MDCP) of the Regulatory Operations and Enforcement Branch oversees post-market compliance and enforcement, recall reporting, inspections, shortage reporting and ...

Urinary levels of non-essential (i.e., cadmium ... assessment in cardiovascular risk prediction, especially for patients in areas with known contamination or occupational exposures." "Until we have ...

And medical information systems and electrocardiographs come out top in IoMT. The top three verticals with the riskiest devices are technology, education, and manufacturing. An example of how ...

UB classifies data into three risk-based categories to regulate access to, use of, and necessary precautions required to the protect university data. This policy provides a classification ... this ...

Additional information on how medical devices are approved and authorized in Canada is available on the fact sheet "Safe Medical Devices in Canada" and the "Classification of ... the scientific and ...

Expert guidance and practical tools to stay ahead of the curve in your IT audit and assurance career ...