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Weekend: 10AM - 5PM
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Insights curated by GLORAMP Pharma Consulting LtdStay informed with the most recent developments from leading global authorities — EMA, MHRA, FDA, CMDh, and EDQM — plus key regulatory shifts affecting pharmaceutical operations, pharmacovigilance, quality systems, eTMF management, and QP batch…

European authorities are tightening requirements around medicine availability and environmental sustainability. What This Means for You: Introduction: EU pharma industry expectate new regulations changes in the year 2025. European Medicines Agency (EMA) and other regulatory authorities in the continent gradually…