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EMA was set up on 1 April 2001 to take over the regulatory functions of the Public Utilities Board, and the operations of the power grid by SP PowerGrid.. It aims to ensure a reliable and secure energy supply, promote effective competition in the energy market and develop a dynamic energy sector in Singapore.
Energy Market Authority (EMA) Enterprise Singapore (EnterpriseSG) Gambling Regulatory Authority of Singapore (GRA) Government Technology Agency (GovTech) Health Promotion Board (HPB) Health Sciences Authority (HSA) Home Team Science and Technology Agency (HTX) Hotels Licensing Board (HLB) Housing and Development Board (HDB) Infocomm Media ...
SP Services – Provides integrated customer billing services for electricity, water and piped gas supplies in Singapore. It holds the nation's Market Support Services License to provide meter reading services, meter data management, and facilitates customers' transfer from the regulated tariff to the Open Electricity Market retailers, or to the wholesale electricity market.
PUB, Singapore's National Water Agency, commonly known as PUB, an acronym for Public Utilities Board, is a statutory board under the Ministry of Sustainability and the Environment of the Government of Singapore responsible for ensuring a sustainable and efficient water supply in Singapore.
The Government of Singapore consists of several departments, known as ministries and statutory boards in Singapore.Ministries are led by a member of the Cabinet and deal with state matters that require direct political oversight.
The Ministry of Trade and Industry (MTI; Malay: Kementerian Perdagangan dan Perusahaan; Chinese: 贸工部; Tamil: வர்த்தக, தொழில் அமைச்சு) is a ministry of the government of Singapore responsible for the formulation and implementation of policies related to the development of business, trade and industry in Singapore.
The European Medicines Agency (EMA) is an agency of the European Union (EU) in charge of the evaluation and supervision of pharmaceutical products. Prior to 2004, it was known as the European Agency for the Evaluation of Medicinal Products or European Medicines Evaluation Agency ( EMEA ).
It was developed by the European Medicines Agency (EMA, Europe), the Food and Drug Administration (USA) and the Ministry of Health, Labour and Welfare (Japan) starting at World Health Organization International Conference of Drug Regulatory Authorities (ICDRA) at Paris in 1989.