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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.
European Medicines Agency (EMA) Patients' and Consumers' (PCWP) Working Party meeting. The Patients and Consumers Working Party (PCWP) will hold its plenary meeting on 2 July 2024 in the morning. European Medicines Agency, Amsterdam, the Netherlands. Start date: 2 July 2024.
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.
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.
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).
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 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).
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.
3 days ago · EMA’s human medicines committee (CHMP) recommended ten medicines for approval at its June 2024 meeting. The committee recommended granting a marketing authorisation for Balversa (erdafitinib), for the treatment of adult patients with unresectable or metastatic urothelial carcinoma, a cancer of the bladder and urinary system.
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.
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.
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 ).
Jun 6, 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.
TOMORROW X TOGETHER have been nominated at prestigious awards, such as the American Music Awards and People’s Choice Awards, and won at the 2022 MTV EMAs (Best Asia Act) and 2023 MTV VMAs (PUSH Performance of the Year).
Discover how EMA works with stakeholders to catalyse new and innovative digital technologies. Talent Development. Learn about EMA’s efforts in nurturing talent and cultivate interest in the energy sector.
3 days ago · San Diego @ Officials from the European Medicines Agency (EMA) discussed the different types of expedited approval pathways available to sponsors of innovative drugs and advanced therapy medicinal products (ATMPs), as well as the various mechanisms for sponsors seeking scientific and regulatory advice at the DIA 2024 Global Annual Meeting on 19 June.
2 days ago · Urothelial carcinoma is the most common form of bladder cancer, the ninth most frequently diagnosed cancer worldwide. In 2022, there were approximately 614,000 new cases of bladder cancer and ...
2 days ago · The ongoing shortage of glucagon-like peptide 1 receptor (GLP-1) agonists such as semaglutide (marketed as Wegovy and Ozempic) is a “major public health concern” that is unlikely to be resolved in 2024, the European Medicines Agency has warned. Speaking at a briefing on 26 June on how the EU is tackling these shortages, the EMA’s executive director, Emer Cooke, said, “Despite our ...
6 days ago · The EMA’s Committee for Medicinal Products for Human Use will begin the formal review process to make a recommendation to the European Commission, with approval expected in H1 2025. Currently, in the EU, ...
