2024
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Energy Market Authority (EMA) is the government agency that drives the advancement of Singapore's energy future that is resilient, sustainable and competitive.
Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 22-25 July 2024. 14 new medicines recommended for approval; another 11 medicines recommended for extension of therapeutic indications. 26 July 2024.
EMA issues a variety of licences to companies and workers in the electricity and gas industries, companies providing district cooling services to gazetted service areas, and to owners of electrical installations.
E-services for electricity and gas worker/installation licence application and other information.
The European Medicines Agency (EMA) facilitates development and access to medicines for countries within the European Union (EU). EMA evaluates applications for marketing authorisation submitted via the centralised procedure, monitors the safety of medicines across their lifecycle and provides information to healthcare professionals and patients.
We regulate Singapore’s electricity, gas industries and district cooling services to ensure fair competition and protect consumers' interests. Read More. Through our work, EMA seeks to build a clean energy future that is resilient, sustainable, and competitive.
Quality Service Manager Line: 1800 734 9177*. Operating hours: 8.00am to 5.30pm, Mondays to Fridays. Closed on Weekends and Public Holidays. * Airtime charges may be imposed by service providers for mobile calls made to 1800 local toll-free numbers.
Factors Influencing Prices. As a resource-constrained country, Singapore relies on imported natural gas for around 95% of our electricity supply. This means that energy developments around the world will impact our domestic electricity prices.
The European Medicines Agency (EMA) is a decentralised agency of the European Union (EU). It is responsible for the scientific evaluation, supervision and safety monitoring of medicines. EMA Working for every patient in Europe (video in English, with subtitles in 24 different languages) ~ 2 mins
The European Medicines Agency (EMA) protects and promotes human and animal health by evaluating and monitoring medicines within the European Union (EU) and the European Economic Area (EEA).
The mission of the European Medicines Agency (EMA) is to foster scientific excellence in the evaluation and supervision of medicines, for the benefit of public and animal health in the European Union (EU).
EMA Elise. We are connecting you to the Singpass service login page. Please wait... You will be automatically re-directed to the Singpass service login page, or click here for immediate re-direction.
What’s new. Find all new and updated information published on our website in one place below. Filters are available to narrow results down based on your interests, such as whether it relates to human or veterinary medicines or specific topics. This overview covers up to two months back. Current month Previous month Two months ago.
The Energy Market Authority (“EMA”) is a statutory board under the Ministry of Trade and Industry. Our main goals are to ensure a reliable and secure energy supply, promote effective competition in the energy market, and develop a dynamic energy sector in Singapore.
The European Medicines Agency (EMA) is a decentralised agency of the European Union (EU) responsible for the scientific evaluation, supervision and safety monitoring of medicines in the EU.
The European Medicines Agency's Committee for Medicinal Products for Human Use prepares scientific guidelines in consultation with regulatory authorities in the European Union (EU) Member States, to help applicants prepare marketing authorisation applications for human medicines.
Jul 25, 2024 · EMA’s human medicines committee (CHMP) recommended 14 medicines for approval at its July 2024 meeting. The CHMP recommended granting a marketing authorisation for Anzupgo (delgocitinib), a medicine intended for the treatment of moderate to severe chronic hand eczema in adults for whom topical corticosteroids are inadequate or inappropriate.
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 ).
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The EMA said that although patients given lecanemab, whose brand name is Leqembi, had delayed cognitive decline, the effects were small. It said the most important safety concern was the frequent ...
EMA regulates Singapore’s electricity, gas industries and district cooling industries through legislation, policies and frameworks and codes of practice and more. Industries Regulated by EMA Below is an overview of the industries that are regulated by EMA:
6 days ago · DISCLOSURES July 26, 2024. 5. 13. In its July 2024 meeting, the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) recommended not granting marketing ...
The Singapore Energy Statistics (SES) is Energy Market Authority (EMA)'s annual online publication on energy statistics in Singapore. It aims to provide users with a comprehensive understanding of the Singapore energy landscape through a detailed coverage of various energy-related topics.
The Energy Market Authority (EMA) is a statutory board under the Singapore Ministry of Trade and Industry. Through our work, we seek to build a clean energy future that is resilient, sustainable, and competitive.
Currently, all residential consumers are eligible to buy electricity at the regulated tariff. For the period from July to September 2024, the tariff rate is 29.88 cents/kWh (without GST), or 32.57 cents/kWh (with GST) . Please visit SP Group’s website for the historical electricity tariff rates.
