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Results found for "federal drug administration"


(Raleigh, N.C.) Today, the federal Food and Drug Administration (FDA) approved the first GIP/GLP-1 called “Zepbound” for the purpose of weight loss.
Published: Thursday, January 18th, 2024 @ 12:54 am By: ENC NOW
(Raleigh, N.C.) Today, the federal Food and Drug Administration (FDA) approved the first GIP/GLP-1 called “Zepbound” for the purpose of weight loss.
 
A group of 22 attorneys general sent a letter to Federal Drug Administration (FDA) Commissioner Dr. Robert Califf asking the agency to reverse its decision to certify retail pharmacies to dispense abortion pills.
Published: Saturday, January 21st, 2023 @ 1:39 pm By: Daily Wire
A group of 22 attorneys general sent a letter to Federal Drug Administration (FDA) Commissioner Dr. Robert Califf asking the agency to reverse its decision to certify retail pharmacies to dispense abortion pills.
 
A company that participated in a federal school lunch program has been accused by the Food and Drug Administration of selling juice with high levels of arsenic and made from rotted fruit.
A company that participated in a federal school lunch program has been accused by the Food and Drug Administration of selling juice with high levels of arsenic and made from rotted fruit.
 
Right to Try is gaining momentum across the country, yet states worry a cumbersome federal approval process will continue to inhibit patients' access to experimental drugs
Right to Try is gaining momentum across the country, yet states worry a cumbersome federal approval process will continue to inhibit patients' access to experimental drugs
 
The platform adopted at this week’s Republican National Convention includes a provision urging Congress to enact “Right to Try” legislation, which allows terminally ill patients the opportunity to use drugs or devices that have yet to gain Federal Drug Administration approval
The platform adopted at this week’s Republican National Convention includes a provision urging Congress to enact “Right to Try” legislation, which allows terminally ill patients the opportunity to use drugs or devices that have yet to gain Federal Drug Administration approval
 

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