As anticipated, Congress swiftly reauthorized four important user fee programmes as part of a bill that was essential to passing...
Read moreOn October 28th, an advisory board to the European Medicines Agency advised restricting the use of a class of medications...
Read moreThe necessity to update and alter the FDA's now-contentious rapid approval strategy is highlighted by the protracted, complicated FDA process...
Read moreThe Centers for Disease Control and Prevention on October 19 advised adults in the United States to take Covid boosters from...
Read moreA total of $38 million has been granted by the US Food and Drug Administration (FDA) in the form of...
Read morePeter Marks, a top official at the Food and Drug Administration, is not tasked with determining if the expense of...
Read moreFollowing a decision by the Food and Drug Administration to broaden its authorization of reformulated shots from Moderna and partners...
Read moreAs anticipated, four important user fee programmes were renewed by Congress for the week ending October 1st as part of...
Read moreThe FDA started a programme ten years ago to increase the role of patients in educating sponsors and regulators on...
Read moreThe three current UK-approved bodies have been joined by DEKRA Certification UK, according to the Medicines and Healthcare Products Regulatory...
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