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Driven by high-profile trial data, the FDA is evaluating expanded indications, higher-dose formats, and oral daily pills
Tirzepatide and Pregnancy Planning The three-to-four-week clearance timeline matters significantly if youre considering pregnancy
Pharmaceutical Executive: How do you see the FDAs intent to take action against non-FDA-approved GLP-1 products affecting the competitive landscape for obesity and diabetes therapies in the near term
Solvents drive up material costs and require specialized, complex, and costly manufacturing facilities that arent easy to build quickly
Recalls & Warnings January 13, 2018 Seller of Depression, Prostate Supplements & More Warned for Manufacturing Violations, Drug Claims On August 21, 2017, the FDA issued a warning letter to Irmo-Vita, LLC, following a facility inspection which found that several of the company's products, including Hysta-Min, Man-Affirm, Phung-EX, and Bacto- EX to be adulterated because they were prepared, packed, or held
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