Guidance on Secondary Packaging of Therapeutic and Medicinal Products

Update: 20 October, 2023

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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File format: PDF

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MD5 Checksum: E76D97AE210AEEAA97B38AE995EFB56A

Publication date: 20 October, 2023

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PDF Link: Guidance on Secondary Packaging of Therapeutic and Medicinal Products PDF