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Good Manufacturing Practice (GMP) is a component of Quality Assurance which helps to ensure that medicinal products are consistently produced with the quality standards appropriate for their intended use. Under the Medicines Act, all manufacturers and assemblers of medicinal products (both Western Medicines and Chinese Proprietary Medicines (CPM)) are required to conform to GMP. As a member of PIC/S, HSAs GMP auditors will conduct audits on medicinal product manufacturers and assemblers in accordance with the PIC/S Guide to GMP for Medicinal Products (Part I) and its relevant annexes, which encompass all the recommendations of the World Health Organization (WHO) in relation to GMP.
GMP Certification Program is designed to verify that manufacturing practices for dietary supplements conform to a standardized set of good manufacturing practices (GMPs) developed and approved by the Natural Products Association in. GMP will improve the health of the individual patient and the community, as well as benefiting the pharmaceutical industry and health professionals. Making and distributing poor quality medicines leads to loss of credibility for everyone: both public and private health care and the manufacturer in.
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ISO 13485:2013 in Surat
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