HSA Invites Feedback on the Proposed Regulation for Active Ingredients under the Health Products Act
The Health Sciences Authority (HSA) invites public feedback on a new piece of legislation known as the proposed Health Products (Active Ingredients) Regulations 2023. The public consultation will run from 17 July 2023 to 17 August 2023, at https://go.gov.sg/airegpublicconsult2023. The public consultation document and draft legislation are available on the HSA website (www.hsa.gov.sg/active-ingredients) and REACH portal (https://go.gov.sg/feedbackaireg2023).
2 Active ingredients are pharmacologically active substances that may be used to manufacture health products, including therapeutic products, cell tissue or gene therapy products, and medical devices. Active ingredients are currently regulated under two different Acts, namely the Poisons Act 1938 and the Medicines Act 1975.
3 With the increasing complexity in the manufacturing and supply chain of active ingredients, streamlined and risk-based regulatory controls will ensure that active ingredients consistently meet the appropriate quality standards. To achieve this, HSA will be consolidating and enhancing the regulatory controls for active ingredients under a single Act, the Health Products Act (HPA). When the proposed Health Products (Active Ingredients) Regulations 2023 is implemented, the regulatory controls of active ingredients under the Poisons Act 1938 and Medicines Act 1975 will no longer apply.
4 HSA’s proposed new regulation of active ingredients aims to achieve the following objectives:
i. To safeguard public health by ensuring that active ingredients are consistently manufactured, stored and distributed with the quality standards appropriate for their intended use.
ii. To provide a fit-for-purpose and risk-based licensing framework that aligns with international standards and enhances mutual confidence with overseas counterparts.
iii. To streamline the regulation of active ingredients under a single legislation through the HPA, providing greater clarity in legal requirements and regulatory controls for all active ingredient manufacturers, importers and wholesalers.
Key proposed legislative changes and regulatory controls
5 The key proposed legislative changes and regulatory controls include:
i. The scope of Active Ingredients regulatory controls. The Health Products (Active Ingredients) Regulations 2023 is proposed to regulate active ingredients that are specified in The Schedule of the Regulations. The scheduled active ingredients are those that are usable as pharmacologically active constituents in the manufacture of any of the following health products:
- Cell Tissue or Gene Therapy Products that are not a result of only minimal manipulation of cell or tissue
ii. Adopting a risk-based regulatory approach for activity-based licensing of manufacturers, importers and wholesalers of active ingredients:
- Inspection and licensing controls will apply to all manufacturers, importers and wholesalers of active ingredients used in health products for local clinical use. Such companies handling active ingredients will be inspected for compliance with the Pharmaceutical Inspection Co-operation Scheme (PIC/S) Good Manufacturing Practice (GMP) Guide or HSA Good Distribution Practice (GDP) standard.
- Importers and/or wholesalers performing lower risk activities such as supplying active ingredients for non-clinical use (e.g., scientific research, use in animals and other applications not involving humans) will be subjected to less stringent requirements. HSA shall reserve the rights to inspect, as required.
- Licensed importers and wholesalers of active ingredients will no longer need to hold separate Form A Poisons Licences under the Poisons Act.
HEALTH SCIENCES AUTHORITY
17 JULY 2023