Tag: CGMP
Contamination Controls: Preventing Adulteration in Generic Drug Manufacturing
Contamination controls in generic drug manufacturing prevent harmful residues and microbes from entering medicines. Learn how cleanrooms, real-time monitoring, and human factors impact drug safety-and what’s changing by 2025.
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Learn the essential documentation requirements for recording generic drug substitutions in pharmacy practice. Understand state laws, what to log, common mistakes, and how to avoid errors that impact patient safety.
Published ON: 1 DecLithium carbonate generics require careful serum level monitoring due to their narrow therapeutic window. Switching between brands can alter blood levels, risking toxicity or relapse. Learn safe targets, testing schedules, and how to avoid dangerous interactions.
Published ON: 1 DecContamination controls in generic drug manufacturing prevent harmful residues and microbes from entering medicines. Learn how cleanrooms, real-time monitoring, and human factors impact drug safety-and what’s changing by 2025.
Published ON: 11 DecDrug interactions occur when medications, foods, or health conditions change how a drug works in your body-potentially causing serious harm or reducing effectiveness. Learn what causes them, who's at risk, and how to prevent dangerous combinations.
Published ON: 3 DecPost-market surveillance uncovers hidden side effects of drugs and medical devices after approval, using real-world data from millions of users. Learn how systems like MedWatch and AI-powered analytics catch dangers clinical trials miss.
Published ON: 5 Dec