December 31, 2025 – PRESSADVANTAGE – As pharmaceutical development becomes increasingly global and highly regulated, pharmacovigilance translation has moved from a supporting function to a central ...
The evaluation of drug safety in clinical trials is a critical element of the drug development process, ensuring that therapeutic benefits outweigh potential harms. Clinical trials, particularly in ...
In a Q&A, an FDA spokesperson discusses efforts to reduce misinformation about biosimilars through education, the agency’s collaboration with global regulators to streamline development, and its work ...
US Food and Drug Administration layoffs appear to be affecting programs that track drug safety. Fired workers from the Division of Drug Information, which conducts safety monitoring, say the DDI team ...
A drug’s therapeutic index is a ratio that doctors use when prescribing medications and determining dosage. It shows how much of a drug a person’s blood can contain before it becomes toxic. The ...
Please provide your email address to receive an email when new articles are posted on . The FDA frequently identifies uncertainties about newly approved cancer drugs, but they are often omitted in ...
Trump cutbacks were supposedly aimed at administrators. But scientists in food and drug-testing labs and policy experts who advance generic drug approvals were also dismissed. By Christina Jewett ...
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