The Good Manufacturing Practice Guides for Licensed Pharmaceutical Manufacturers and Licensed Secondary Packaging Manufacturers

The Pharmacy and Poisons Board of Hong Kong (“the Board”) has issued The Good Manufacturing Practice Guides for Licensed Pharmaceutical Manufacturers and Licensed Secondary Packaging Manufacturers. The Guides are available at the following links:

• Hong Kong Guide to Good Manufacturing Practice for the Secondary Packaging of Pharmaceutical Products (with effect from 1 October 2015 to 30 June 2025)
• Hong Kong Guide to Good Manufacturing Practice for the Secondary Packaging of Pharmaceutical Products (July 2024 version) with effect from 1 July 2025)
• Part I, Part II and Annexes of the Guide to Good Manufacturing Practice for Medicinal Products (PE 009-11) published by the Pharmaceutical Inspection Co-operation Scheme (with effect from 1 October 2015 to 30 June 2025) (English only)
• Part I, Part II and Annexes of the Guide to Good Manufacturing Practice for Medicinal Products (PE 009-17) published by the Pharmaceutical Inspection Co-operation Scheme (with effect from 1 July 2025) (English only) (English only)

Please contact the Drug Office of the Department of Health at 2961 8028 for enquiries.