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BioWorld - Wednesday, December 10, 2025
Home » Topics » Regulatory

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Regulatory front

July 5, 2019
In an ongoing crackdown on repackers, the FDA recently issued warning letters to three repackers of active pharmaceutical ingredients (API) for significant violations of current good manufacturing practice requirements.
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FDA grants accelerated approval to Xpovio for relapsed refractory multiple myeloma

July 4, 2019

FDA warning letters decline under Trump, inspections increase

July 3, 2019
By Mari Serebrov
The FDA's Center for Drug Evaluation and Research (CDER) issued 62% more warning letters under the first part of the Trump administration than it did during the last few years of the Obama administration. But the number of warnings for medical devices, food and tobacco products fell sharply under President Donald Trump, according to an investigative report being published in the July 5 issue of Science.
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Regulatory front

July 2, 2019
The FDA Monday released two draft guidances on the content and format of specific sections in prescription drug labeling. 
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Danish Medicines Agency approves AJ Vaccines' polio vaccine

July 1, 2019

FDA approves Soliris for neuromyelitis optica spectrum disorder

June 28, 2019

Dupixent obtains U.S. approval for chronic rhinosinusitis with nasal polyposis

June 27, 2019

FDA approves Vyleesi for hypoactive sexual desire disorder in premenopausal women

June 25, 2019

FDA greenlights Cochlear's Nucleus Profile Plus series with greater MRI access, expanded connectivity

June 24, 2019
By Meg Bryant
Cochlear Ltd., of Sydney, received U.S. FDA approval for its Nucleus Profile Plus cochlear implant and the Nucleus 7 sound processor's new built-in connectivity, enabling direct streaming with compatible Android smartphones. The implant will be commercially available in the U.S. later this month.
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Japan first to approve Breztri Aerosphere for COPD

June 19, 2019
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