Guidance on Secondary Packaging of Therapeutic and Medicinal Products

This document is a guidance for industry issued by the Health Sciences Authority of Singapore, which provides regulatory requirements and GMP requirements for secondary packaging of therapeutic and medicinal products, including requirements for manufacturer's licence, application for manufacturer's licence and GMP certificate, obligations and responsibilities of licensed secondary packagers.

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PDF
Published
20 October, 2023
Updated
20 October, 2023
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E76D97AE210AEEAA97B38AE995EFB56A
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Guidance on Secondary Packaging of Therapeutic and Medicinal Products PDF
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