The Health Sciences Authority (HSA) Singapore has published the first version of the guidelines on manufacturing standards of traditional medicines (TM) and health supplements (HS) in March 2022.
Manufacturers are required to provide some evidence of the manufacturing standards for their TM and HS. The information that can be provided include manufacturer’s license and Good Manufacturing Practice certification issued by the relevant regulatory authority.
Third party certification can also be included if accredited by the Singapore Accreditation Council (SAC) or other accreditation bodies listed under the SAC’s Mutual Recognition Agreement (MRA).
More details can be found in “Guidelines for Manufacturing Standards of Traditional Medicines and Health Supplements, March 2022”: https://www.hsa.gov.sg/docs/default-source/hprg-tmhs/chpb-tmhs/tmhs_manufacturing_guidelines.pdf