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Singapore medicines regulator world’s first to achieve highest maturity level in WHO classification

Regulatory authorities that reach maturity levels three and four will be considered eligible for inclusion among WHO-listed authorities, after additional evaluation of their performance

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Out of 28 countries formally assessed by the World Health Organization (WHO), Singapore is the first to have achieved the highest maturity level (ML 4) in WHO’s classification of regulatory authorities for medical products. Achieving ML 4 brings Singapore closer to becoming a WHO-listed authority, a new scheme that will be operational later this year and will list the world’s regulators of reference, WHO notified in a statement.

“This is great recognition of Singapore’s achievement and very good news for the broader region. Singapore already helps several neighbouring countries to expedite their medicines assessments and this WHO classification may also encourage other countries and areas to continue strengthening their medicines oversight,” said Martin Taylor, Western Pacific Region Director of Health Systems and Services and acting Director for Data, Strategy and Innovation, WHO, in the statement.

Regulation of medical products is important for all health systems and for access to quality vaccines, medicines and other health products. Apart from ensuring the quality, safety and efficacy of medical products, regulatory authorities that function well also perform critical functions such as faster authorisation of products and drug safety monitoring after authorisation, said the statement.

It also mentioned that WHO’s assessment of regulatory authorities is based on the ‘Global Benchmarking Tool’ – an evaluation tool that checks regulatory functions against a set of more than 260 indicators – covering core regulatory functions such as product authorisation, testing of products, market surveillance and the ability to detect adverse events – to establish their level of maturity and functionality. Regulatory authorities that reach maturity levels three and four will be considered eligible for inclusion among WHO-listed authorities, after additional evaluation of their performance.

The benchmarking of Singapore’s Health Sciences Authority (HSA) was carried out by a WHO-led team of international experts. In late 2021, WHO conducted a formal evaluation of the authority and the HSA was found to perform well against the indicators of the Global Benchmarking Tool, it further added.

“The Health Sciences Authority of Singapore is honoured to have achieved maturity level four in WHO’s recent global benchmarking assessment. This achievement is a significant milestone and affirmation for Singapore as the first WHO member state to have reached this highest maturity level for our medicines regulatory system. I believe this achievement will boost public confidence and trust in the system. I look forward to HSA sustaining our culture of operational excellence and continuous improvement and continuing our strong collaboration with WHO in regulatory systems strengthening,” said Dr Choong May Ling, Mimi, Chief Executive Officer, Health Sciences Authority, Singapore, in the statement.

It also noted that fewer than 30 per cent of the world’s medicines regulatory authorities are considered to have the capacity to perform the functions required to ensure medicines, vaccines and other health products work and do not harm patients. For that reason, WHO has intensified efforts to bolster the capacity to regulate medical products in all regions and is working to strengthen regulatory networks where the most advanced regulatory authorities can act as lighthouses for regulators with fewer resources or which have not yet reached maturity.

“The core of WHO’s work is to empower countries through support and knowledge sharing so that they can expand access to health services for their populations. If countries want to improve health outcomes, if they want to be able to address health emergencies and expand local production, they first need to be able to ensure access to safe and quality medical products that actually work and benefit patients,” said Mariângela Simão, Assistant Director-General for Access to Medicines and Other Health Products, WHO, in the statement.

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