The US Food and Drug Administration (FDA) announced on Tuesday the launch of a pilot program designed to expedite the review ...
Experts in medical device and pharmaceutical regulatory affairs discussed how the field has evolved over the last five ...
Heidi Overton, President Donald Trump’s nominee to lead the US Food and Drug Administration (FDA), faced questions from both sides of the political aisle about her views on hot-button issues facing ...
A panel of experts representing the European Commission, industry, and notified bodies reviewed the state discussed the ...
Officials from the US Food and Drug Administration (FDA), the European Medicines Agency (EMA), and industry representatives ...
Welcome to Regulatory Reconnaissance, your regulatory news and intelligence briefing.
Welcome to Regulatory Reconnaissance, your regulatory news and intelligence briefing.
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 ...
This week, a Senate committee scheduled a hearing for President Trump’s nominee to lead FDA, new reporting sheds light on the ...
Welcome to Regulatory Reconnaissance, your regulatory news and intelligence briefing. In Foc ...
Commissioner Robert Califf was a medical student in the mid-1970s, he had an opportunity to work with his mentor on one of ...
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