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GS1 standards to support U.S. FDA medical device regulation
WASHINGTON | The U.S. Food and Drug Administration has issued its final ruling requiring manufacturers to implement a unique device identification system for their products. This includes the use of a unique identifier on the label of medical device packaging. -
MEDEC: We helped Health Canada revise position on medical devices
TOROTNO | MEDEC, the national association for Canadian medical technology industry, is commending the decision by Health Canada to revise its position on how the purchase of medical devices for use in healthcare facilities is handled in requests for proposals (RFPs) and requests for information (RFIs) under the Medical Devices Regulations.