The Office of the Taxpayers' Ombudsperson (OTO) works independently from the Canada Revenue Agency (CRA). We are here to improve the service that the CRA provides to taxpayers by reviewing ...

The FDA reached a significant milestone when it approved its reorganization and created its new unified Human Foods Program ...

But ensuring the free flow of data across borders involves navigating complex regulatory, security, trust, political, and technical challenges. Developing effective frameworks and agreements to ...

Now, the U.S. Food and Drug Administration (FDA) is working on a new study to get to the bottom of this issue and better understand how these metals are affecting women’s health. The decision ...

who also ran government affairs at blockchain analytics firm Chainalysis, said in a Friday statement. "The ever-evolving legislative and regulatory landscape will continue to require strong ...

In October 2022, the FDA established over-the-counter hearing aid regulations allowing consumers to purchase the devices in stores, versus at a physician's office, making it easier for many to ...

The FDA continues to investigate six ongoing outbreaks from foodborne pathogens, with increasing patient counts in four of the six. This week, the Food and Drug Administration confirmed reports ...

The FDA on Thursday said its marketing authorization of the product was its first ever for a over-the-counter hearing aid software device. Related Apple to release AirPods with built-in hearing ...

The FDA approved the software device, “Hearing Aid Feature,” which the agency said could be installed on Apple’s AirPods Pro headphones to amplify sounds for anyone 18 or older with mild to ...

Just days after Apple announced a new hearing aid feature for the second-generation AirPods Pro, the US Food and Drug Administration (FDA) has authorized the software that powers this functionality.

Apple will soon allow the AirPods Pro 2 to serve as an over-the-counter hearing aid, and the company has now received FDA clearance for the feature. As noted by TechCrunch, the FDA today announced ...

FDA should take steps to make information publicly available and accessible on authorization submissions, review milestones, negative reviews and approvals, and the use of regulatory flexibilities for ...