The European Union (EU) has implemented stringent regulations and quality standards for the importation of pharmaceutical products to ensure patient safety and product efficacy. Two critical aspects of this regulatory framework are the EU Batch Release and Good Manufacturing Practice (GMP) requirements. In this blog post, we will explore the significance of EU Batch Release and GMP requirements for the importation of pharmaceuticals into the EU market.
Read MoreComputerized System Validation is crucial in the pharmaceutical sector to ensure the operational efficiency of electronic systems. It is a continuous process that begins with identifying the functional requirements and involves comprehensive testing to confirm that the system remains reliable and compliant with regulatory requirements.
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