Search results
Jun 4, 2024 · Energy Market Authority (EMA) is the government agency that drives the advancement of Singapore's energy future that is resilient, sustainable and competitive.
E-services for electricity and gas worker/installation licence application and other information.
EudraVigilance is the EU's system for managing and analysing information on adverse reactions to medicines which have been authorised or are being studied in clinical trials in the European Economic Area (EEA) and supports the reporting and analysis of suspected adverse reactions originating from clinical trials and the post-authorisation phase of.
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.
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) 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 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
