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European Medicines Agency Company Profile

17:52 EDT 20th September 2017 | BioPortfolio

European Medicines Agency (EMEA) is a decentralised body of the European Union with headquarters in London.ts main responsibility is the protection and promotion of public and animal health, through the evaluation and supervision of medicines for human and veterinary use. The EMEA coordinates the evaluation and supervision of medicinal products throughout the European Union. The Agency brings together the scientific resources of the 25 EU Member States in a network of 42 national competent authorities. It cooperates closely with international partners, reinforcing the EU contribution to global harmonisation.

Location

7 Westferry Circus | Canary Wharf
London
London
E14 4HB
United Kingdom

Contact

Phone: 44-20) 74 18 84 00
Fax: 44-20) 74 18 84 16
Email: info@emea.eu.int


News Articles [3092 Associated News Articles listed on BioPortfolio]

Germany eyes European Medicines Agency after Brexit

Germany said Wednesday it would apply for the European Medicines Agency (EMA) to move from London to Bonn after Brexit, pitting the western city against EU competitors from Helsinki to Barcelona.

Ireland steps up bid for European Medicines Agency

As European Union leaders prepare for Brexit negotiations with the UK, Ireland has stepped up its bid to make Dublin the new home of the EU’s medicines agency. The EMA looks virtually certain to ...

Roche's Tecentriq receives positive opinion from EU medicines agency

ZURICH (Reuters) - A European Medicines Agency (EMA) panel said on Friday it has recommended Roche's immunotherapy Tecentriq as a treatment for advanced bladder and lung cancer, setting the stage for ...

How the EU regulates medicines

The European Medicines Agency (EMA) will host an awareness session to present the European Union’s (EU) medicines regulatory system and EMA's role in it to international regulators and non-governmen...

EU and USA in Medicines Inspections Pact

The European Commission, the European Medicines Agency (EMA) and the US Food and Drug Administration (FDA) have signed an agreement enabling them to share non-public and commercially confidential info...

Ireland reiterates bid to host the European Medicines Agency

Ireland has stepped up its bid to host the European Medicines Agency (EMA) with the official announcement…

European Medicines Agency recommends approval of Humira biosimilar Imraldi

The European Medicines Agency’s (EMA) Committee for Medicinal Products for Human Use (CHMP) has recommended Samsung Bioepis' Imraldi for approval, which is a biosimilar candidate referencing Humira ...

EMA prepares for Brexit

The European Medicines Agency (EMA) has developed and initiated a business continuity plan to deal with the uncertainty and workload implications linked to the United Kingdom’s (UK’s) withdrawal f...

Drugs and Medications [169 Associated Drugs and Medications listed on BioPortfolio]

Terbinafine hydrochloride [Aurobindo Pharma Limited]

These highlights do not include all the information needed to use terbinafine hydrochloride safely and effectively. See full prescribing information for terbinafine hydrochloride tablets.Terbinafine H...

Cimetidine [Walgreen Company]

Walgreen Co. Cimetidine 200 Drug Facts

Dg health heartburn relief [Dolgencorp, LLC]

Dolgencorp, LLC Heartburn Relief Drug Facts

Acid reducer [Rite Aid Corporation]

Rite Aid Corporation Acid Reducer Drug Facts

Smart sense acid reducer [Kmart Corporation]

Kmart Corporation Acid Reducer Drug Facts

PubMed Articles [2448 Associated PubMed Articles listed on BioPortfolio]

The European Medicines Agency and Publication of Clinical Study Reports: A Challenge for the US FDA.

RUMA adopts European Medicines Agency's list of highest priority antibiotics.

Affordability of medicines in the European Union.

Medications and their prices are key issues for healthcare. Although access to medicines at affordable prices had been specified as a key objective of the European Health Policy, it seems that these g...

TRANSPARENCY POLICIES OF THE EUROPEAN MEDICINES AGENCY: HAS THE PARADIGM SHIFTED?

This article reflects on the state of play as regards access to non-summary clinical trial data in the European Union (EU). In particular, it examines the scope of access under the recent transparency...

A randomized Phase II/III study of cabazitaxel versus vinflunine in metastatic or locally advanced transitional cell carcinoma of the urothelium (SECAVIN).

Despite the advent of immunotherapy in urothelial cancer, there is still a need to find effective cytotoxic agents beyond first and second line. Vinflunine is the only treatment approved in this setti...

Clinical Trials [952 Associated Clinical Trials listed on BioPortfolio]

PENTA Fosamprenavir Study

Twice daily fosamprenavir, in combination with low dose ritonavir (FPV/RTV BID), is indicated for the treatment of HIV-infected adults, adolescents and children of 6 years of age and above...

Study of Talimogene Laherparepvec in Pancreatic Cancer

The purpose of this study is to find out which doses of talimogene laherparepvec (T-Vec) can be given safely to participants with pancreatic cancer that is either too big to be taken out b...

A Randomized Acceptability and Safety Study of the Transfer From Subutex to Suboxone in Opioid- Dependent Subjects (Study P04843)(COMPLETED)

Post-marketing commitment to the European Medicines Agency to conduct a prospective, controlled study of the transfer from Subutex to Suboxone.

A Non-interventional Study to Identify the Patients With Severe Luteinizing Hormone Deficiency in the Daily Practice

This non-interventional study is planned to identify the subjects with severe luteinizing hormone (LH) deficiency in the daily practice. The results will be used for the "Periodic Safety U...

Study of GSK Biologicals' Pandemic Influenza (H1N1) Candidate Vaccine in Children Aged 10 to Less Than 18 Years

The purpose of this study is to show that vaccination with a single dose of GSK Biologicals' pandemic H1N1 vaccine results in an immune response that meets or exceeds European Medicines Ag...

Companies [1517 Associated Companies listed on BioPortfolio]

European Medicines Agency

European Medicines Agency (EMEA) is a decentralised body of the European Union with headquarters in London.ts main responsibility is the protection and promotion of public and animal health, through t...

European Medicines Evaluation Agency (EMEA)

European Medicines Evaluation Agency (EMEA)

European Generic medicines Association

The EGA is the official representative body of the European generic pharmaceutical industry, which is at the forefront of providing high-quality affordable medicines to millions of Europeans and stimu...

European Directorate for the Quality of Medicines

The EDQM was created in 1996 and is a Directorate of the Council of Europe. Its premises have been especially designed for its various activities. Today the EDQM is organised into nine administrative...

Australia New ZealandTherapeutic ProductsAuthority

The trans Tasman therapeutic products agency project has involved New Zealand and Australia giving consideration to establishing a joint agency to regulate therapeutic products (medicines, medical dev...

More Information about "European Medicines Agency" on BioPortfolio

We have published hundreds of European Medicines Agency news stories on BioPortfolio along with dozens of European Medicines Agency Clinical Trials and PubMed Articles about European Medicines Agency for you to read. In addition to the medical data, news and clinical trials, BioPortfolio also has a large collection of European Medicines Agency Companies in our database. You can also find out about relevant European Medicines Agency Drugs and Medications on this site too.

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