The "cGMP Regulatory Inspections - Through the Eyes of FDA, EMA and PMDA (Nov 13, 2025)" training has been added to ResearchAndMarkets.com's offering. cGMP or current good manufacturing practices are ...
The FDA's streamlined approval processes, including updated 510(k) and De Novo pathways and innovative programs like the Breakthrough Device and Safer Technologies Programs, present opportunities for ...
DUBLIN--(BUSINESS WIRE)--The "Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems Course" training has been added to ResearchAndMarkets.com's offering. This ...
Frank Romanski of Lonza Capsugel dives into the excipient side of manufacturing and the emerging prevalence of digitalization ...
The U.S. Food and Drug Administration has issued a recall on deodorant sold online and at several major retail chains countrywide. In total, over 67,000 cases of three different types of deodorant ...
This milestone marks the approval of the first product to get U.S. FDA clearance for commercial supply from Kemwell’s Bengaluru drug-product facility since the site became a dedicated biologics campus ...
The U.S. Food and Drug Administration has flagged three of Philips' medical device facilities after inspections found they ...
As discussions intensify about how the second Trump administration will reshape the regulatory landscape for U.S.-based life sciences firms, less attention has been given to the new administration’s ...
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