The US Food and Drug Administration (FDA) announced on Tuesday the launch of a pilot program designed to expedite the review ...
The US Food and Drug Administration (FDA) announced on Tuesday the launch of a pilot program designed to expedite the review ...
The US Food and Drug Administration (FDA) recently issued warning letters to ophthalmic product maker Bausch and Lomb and an Indian active pharmaceutical ingredient (API) maker for violations of good ...
The European Medicines Agency (EMA) has published a guideline on evaluating drug interactions in the gastrointestinal tract ...
The US Food and Drug Administration (FDA) has notified more than 2,200 medical product manufacturers and researchers to disclose clinical trial results as required by law. The agency said it is part ...
Regulatory Recon is our regular intelligence briefing for the regulatory affairs space, bringing you the top regulatory, ...
Singapore’s Parliament has advanced legislation to build “a more coherent, future-ready system” that provides clarity and ...
A recent report from the European Medicines Agency (EMA) highlights that global regulators are strongly committed to sharing ...
Top US Food and Drug Administration (FDA) officials said the agency is open to novel, “innovative approaches” to the clinical ...
The US Food and Drug Administration (FDA) has announced the permanent appointment of four top officials to lead the agency's ...
Industry stakeholders want the US Food and Drug Administration (FDA) to expand the scope of its recent draft guidance on the ...
Welcome to another installment of This Week at FDA, your weekly source for updates – big and small – on FDA, drug, and ...
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