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Jun 5, 2024 · Energy Market Authority (EMA) is the government agency that drives the advancement of Singapore's energy future that is resilient, sustainable and competitive.
Featured news and updates for patients and carers. Featured news and updates for healthcare professionals, including doctors, nurses and pharmacists. Featured news and updates for animal health professionals and users of veterinary medicines such as pet owners.
E-services for electricity and gas worker/installation licence application and other information.
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.
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.
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 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.
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) protects and promotes human and animal health by evaluating and monitoring medicines within the European Union (EU) and the European Economic Area (EEA).
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
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 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).
With over 7,000 Members, we are New Zealand’s largest business association. We are at the forefront of the business environment, advocating for, and providing support, advice, representation and training to our member organisations. 0800 300 362.
Discover the different legislations which allow EMA to make, amend and enforce regulations for the electricity, gas and district cooling services industries. Gain insights into the policies and frameworks that EMA introduces to keep pace with the changing environment in the energy market.
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 ).
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. What's new - Menu tabs.
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.
EMA does not have a role in the authorisation of clinical trials in the EU; this is the responsibility of the national competent authorities. However, EMA, in cooperation with the EU Member States, plays a key role in ensuring that medicine developers follow EU and international standards.
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.
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.
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.
Jun 28, 2024 · EMA’s human medicines committee ( CHMP) has concluded its review of the medicine Ocaliva (obeticholic acid) and has recommended that the medicine’s marketing authorisation be revoked, because its benefits are no longer considered to outweigh its risks. Ocaliva is used to treat adults with primary biliary cholangitis (PBC), an autoimmune ...
Jul 8, 2024 · The Energy Market Authority (EMA) has called for proposals for two more hydrogen-compatible natural gas power plants, each with a capacity of at least 600 MW. When completed, this will bring the total number of hydrogen-compatible plants in Singapore to nine, producing over 3.7 gigawatts (GW) of power.
May 31, 2024 · RENOVATION WORKS FOR EMA'S OFFICE AT AYER RAJAH (EMA-ITT-2024-0036) Email. Print. OPEN. The information contained within the procurement notices/documents is intended for the sole purpose of suppliers preparing for their bids, and shall be used only for this intended purpose.
Manufacturing and Importation Authorisations are to be entered into EudraGMDP, as referred to in article 40 (4) of Directive 2001/83/EC as amended, and article 88 (4) of Regulation (EU) 2019/6. The EudraGMDP database is maintained and operated by the EMA. Access to the general public is granted in order to enhance availability of information ...
