2024
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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.
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.
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.
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.
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 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.
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 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).
Jun 11, 2024 · The Energy Market Authority (EMA) has commissioned a new Energy Management System (EMS) with advanced tools and capabilities to better monitor and control Singapore's electricity transmission network and generating plants, as well as monitor the natural gas transmission network.
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
Corporate Services Division. Oversees corporate development and services for EMA divisions while driving organisational excellence and transformation, including enhancing the professional capabilities and capacity within EMA.
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.
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 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).
3 days ago · Address : 991G Alexandra Road #01-29 & #02-29 Singapore 119975. Tel. 68358000. Fax. 68358020. http://www.ema.gov.sg. ema_enquiry@ema.gov.sg. To Forge a Progressive Energy Landscape for Sustained Growth.
An EMA licence is required to use or operate an electrical installation of approved load exceeding 45 kVA for non-domestic purposes. Electrical installations in premises used for "hazardous trades", irrespective of their approved loads, are also required to be licensed.
Worker Licence Application Requirements. Application for an Electrical Technician's Licence. An electrical technician's licence entitles the holder to carry out the following electrical work ; (a) install, repair, maintain, operate, inspect and test an electrical installation where the operating voltage of such installation does not exceed 1000 ...
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 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.
Authorisation of medicines. All medicines must be authorised before they can be marketed and made available to patients. In the European Union (EU), there are two main routes for authorising medicines: a centralised route and a national route. Corporate.
3 days ago · EMA and the Heads of Medicines Agencies (HMA), through the Executive Steering Group on Shortages and Safety of Medicinal Products (MSSG), have issued recommendations to tackle shortages of the glucagon-like peptide-1 (GLP-1) receptor agonists Ozempic (semaglutide), Saxenda (liraglutide), Trulicity (dulaglutide) and Victoza (liraglutide).
May 30, 2024 · EMA is the first regulatory authority worldwide to provide such broad access to clinical data. For more information on the clinical data on this website, see Clinical data available. For more information on EMA and its policy on the publication of clinical data, see the EMA corporate website.
2 days ago · Ever since Novo Nordisk published data showing significant weight loss effects, there has been a surge in demand for so-called GLP-1 receptor agonists, a class of drugs used to treat type 2 diabetes and obesity, leading to shortages since 2022.. While manufacturing constraints are part of the reason, the EMA also blamed off-label use of the drugs for the shortfall, which it said was likely to ...
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 ).
