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Getting Your Medical Device Into the US Market The White Paper provides real-world and practical information directed to the manufacturer of Class II and Class III devices in navigating the Premarket Notification 510(k) clearance with insight into the various documentation required by FDA for submitting a 501(k) FDA Issues New Food Defense Guide, Food Safety Software FDA released two useful tools last month to advise and assist companies in complying with new FSMA rules

With the demand for hemp-derived products growing and the flexibility of distribution, the Redwood family began producing CBD with high health and quality standards

If much of the tobacco is left (the white part), then it is not a butt

Ironically, this is happening despite a broad scientific consensus that vaping products are significantly less harmful than traditional cigarettes