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IPA questions FAERS data interpretation in the Ohio State University study

Express Pharma

IPA also pointed out that US regulations require adverse events related to any dosage form of a drug to be reported under the same Abbreviated New Drug Application (ANDA) number, even if the product is manufactured at a different facility or outside India. Thus, it cannot be conclusively linked with the manufacturing site or manufacturers.

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How Long Until AI Starts to Replace Pharmacists

pharmacy mentor

By leveraging AI, pharmacies can already optimise drug dispensing processes, improve medication management, and enhance patient safety. Dosage Recommendations : AI tools such as Dosis can analyse patient-specific data (e.g. allergies to certain ingredients, paediatric dosages) involves precise techniques and human expertise.